NDC properties for "sulindac 200 MG Oral Tablet" (RxCUI 198239)
About this data
The tables show NDC propoerties for sulindac 200 MG Oral Tablet with the RxCUI 198239
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for sulindac 200 MG Oral Tablet (RxCUI 198239)
| ANDA | ANDA071795 |
|---|---|
| ANDA | ANDA072051 |
| ANDA | ANDA072711 |
| ANDA | ANDA073262 |
| MMSL_CODE | BD3260 |
| MMSL_CODE | CD3260 |
| RxCUI | 198239 |
| SNOMEDCT | 329888005 |
| SPL_SET_ID | 0feabf47-8d0d-48c0-b263-43db4969f39e |
| SPL_SET_ID | 145a1b4a-16ef-4f29-b47e-f52c47514c9a |
| SPL_SET_ID | 1fffe88d-50c8-45cf-ac7c-a62b665c89a8 |
| SPL_SET_ID | 41c7882e-530a-4ac1-8de4-8d1e7b391467 |
| SPL_SET_ID | 6041acc2-5e8a-4d3c-bf50-7e9447748e2b |
| SPL_SET_ID | 68d4eeed-2501-494b-b979-502720de86c0 |
| SPL_SET_ID | 6db52fd3-172f-47ab-8aa6-4f3d031c6b25 |
| SPL_SET_ID | 7a0afa8a-9660-453b-a47d-29c20a8d2d6b |
| SPL_SET_ID | 87449866-cf27-4c2f-b57b-a967408e0d63 |
| SPL_SET_ID | 89b01ca5-cfa5-4f5d-be6b-927d58cce0f2 |
| SPL_SET_ID | 96c73bd2-4577-487d-a642-bd8f91e94c3a |
| SPL_SET_ID | a399a9e2-5413-434c-ae1a-26ac7b796082 |
| SPL_SET_ID | a47e4259-d44b-4b7b-b517-841cb6840982 |
| SPL_SET_ID | b5b9be81-f0b8-4ee2-bcfd-38fbe3805c06 |
| SPL_SET_ID | b8b549e9-53ec-407a-a505-b652faf8f3b6 |
| SPL_SET_ID | b906d325-27f1-4fb4-86ab-a2c896470e1e |
| SPL_SET_ID | c17e8534-4e71-4166-a4fc-9df6cf6dd49b |
| SPL_SET_ID | d8b9d517-5dd4-4c6b-8aa0-736bce87e7b4 |
| SPL_SET_ID | d94e8865-d151-4fb1-bacd-f4e43819e3c2 |
| SPL_SET_ID | ddbbaada-f55a-4032-a24c-a8c493933a45 |
| SPL_SET_ID | df5f89a8-70b3-40bc-8a05-8daa8c881d06 |
| SPL_SET_ID | f4985b1b-7e2c-4911-897a-94c337794bab |
| VUID | 4002975 |
| Prescribable Synonym | sulindac 200 MG Oral Tablet |
| RXNAV_STR | sulindac 200 MG Oral Tablet |
| RxNorm Name | sulindac 200 MG Oral Tablet |
| Related queries | Interactions (for RxCUI 198239) |
NDC Properties
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 00378053101
| NDC 9 | 0378-0531 |
|---|---|
| NDC 10 | 0378-0531-01 |
| NDC Item | 00378053101 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0531-01) |
| ANDA | ANDA073039 |
| COLORTEXT | YELLOW(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 571333 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-06-30 |
| Marketing effective time low | 1993-06-22 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0378-0531 |
NDC Item 00591566001
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-01 |
| NDC Item | 00591566001 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5660-01) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00591566005
| NDC 9 | 0591-5660 |
|---|---|
| NDC 10 | 0591-5660-05 |
| NDC Item | 00591566005 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5660-05) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 838697 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Actavis Pharma, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 0591-5660 |
NDC Item 00904733560
| NDC 9 | 0904-7335 |
|---|---|
| NDC 10 | 0904-7335-60 |
| NDC Item | 00904733560 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7335-60) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 862124 |
| Imprint code | MP;116 |
| Labeler | Major Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-07-27 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 0904-7335 |
NDC Item 24658077101
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-01 |
| NDC Item | 24658077101 |
| Packaging | 100 TABLET in 1 BOTTLE (24658-771-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 24658077105
| NDC 9 | 24658-771 |
|---|---|
| NDC 10 | 24658-771-05 |
| NDC Item | 24658077105 |
| Packaging | 500 TABLET in 1 BOTTLE (24658-771-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 756082 |
| Imprint code | E11 |
| Labeler | PuraCap Laboratories LLC dba Blu Pharmaceuticals |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2016-11-14 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 24658-771 |
NDC Item 42806001101
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-01 |
| NDC Item | 42806001101 |
| Packaging | 100 TABLET in 1 BOTTLE (42806-011-01) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001105
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-05 |
| NDC Item | 42806001105 |
| Packaging | 500 TABLET in 1 BOTTLE (42806-011-05) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 42806001110
| NDC 9 | 42806-011 |
|---|---|
| NDC 10 | 42806-011-10 |
| NDC Item | 42806001110 |
| Packaging | 1000 TABLET in 1 BOTTLE (42806-011-10) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 844548 |
| Imprint code | E11 |
| Labeler | Epic Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 42806-011 |
NDC Item 49999065630
| NDC 9 | 49999-656 |
|---|---|
| NDC 10 | 49999-656-30 |
| NDC Item | 49999065630 |
| ANDA | ANDA071795 |
| COLORTEXT | yellow(yellow) |
| Color | C48330 __ |
| FDA SPL set id | 22256 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Lake Erie Medical DBA: Quality Care Products LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-06-23 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shapetext | round |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 49999-656 |
NDC Item 50090052901
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-1 |
| NDC Item | 50090052901 |
| Packaging | 30 TABLET in 1 BOTTLE (50090-0529-1) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090052904
| NDC 9 | 50090-0529 |
|---|---|
| NDC 10 | 50090-0529-4 |
| NDC Item | 50090052904 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-0529-4) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 369158 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-0529 |
NDC Item 50090209304
| NDC 9 | 50090-2093 |
|---|---|
| NDC 10 | 50090-2093-4 |
| NDC Item | 50090209304 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-2093-4) |
| ANDA | ANDA072051 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 753034 |
| Imprint code | MP;116 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 50090-2093 |
NDC Item 50090497604
| NDC 9 | 50090-4976 |
|---|---|
| NDC 10 | 50090-4976-4 |
| NDC Item | 50090497604 |
| Packaging | 60 TABLET in 1 BOTTLE (50090-4976-4) |
| ANDA | ANDA072711 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 593136 |
| Imprint code | E11 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-11-30 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 50090-4976 |
NDC Item 51079066701
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-01 |
| NDC Item | 51079066701 |
| Packaging | 1 in 1 BLISTER PACK |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 51079066720
| NDC 9 | 51079-667 |
|---|---|
| NDC 10 | 51079-667-20 |
| NDC Item | 51079066720 |
| Packaging | 100 BLISTER PACK in 1 CARTON (51079-667-20) / 1 TABLET in 1 BLISTER PACK (51079-667-01) |
| ANDA | ANDA073039 |
| COLORTEXT | yellow(yellow-orange) |
| Color | C48330 __ |
| FDA SPL set id | 440216 |
| Imprint code | MYLAN;531 |
| Labeler | Mylan Institutional Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time high | 2021-03-31 |
| Marketing effective time low | 1997-02-04 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 51079-667 |
NDC Item 52959019514
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-14 |
| NDC Item | 52959019514 |
| Packaging | 14 TABLET in 1 BOTTLE, PLASTIC (52959-195-14) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019515
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-15 |
| NDC Item | 52959019515 |
| Packaging | 15 TABLET in 1 BOTTLE, PLASTIC (52959-195-15) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019518
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-18 |
| NDC Item | 52959019518 |
| Packaging | 18 TABLET in 1 BOTTLE, PLASTIC (52959-195-18) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019520
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-20 |
| NDC Item | 52959019520 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (52959-195-20) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019528
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-28 |
| NDC Item | 52959019528 |
| Packaging | 28 TABLET in 1 BOTTLE, PLASTIC (52959-195-28) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019530
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-30 |
| NDC Item | 52959019530 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (52959-195-30) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 52959019560
| NDC 9 | 52959-195 |
|---|---|
| NDC 10 | 52959-195-60 |
| NDC Item | 52959019560 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (52959-195-60) |
| ANDA | ANDA071795 |
| COLORTEXT | YELLOW |
| Color | C48330 __ |
| FDA SPL set id | 56844 |
| Imprint code | DAN;DAN;5660 |
| Labeler | H.J. Harkins Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 52959-195 |
NDC Item 53489047901
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-01 |
| NDC Item | 53489047901 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-479-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047902
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-02 |
| NDC Item | 53489047902 |
| Packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-479-02) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047903
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-03 |
| NDC Item | 53489047903 |
| Packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-479-03) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047905
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-05 |
| NDC Item | 53489047905 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-479-05) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047906
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-06 |
| NDC Item | 53489047906 |
| Packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-479-06) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 53489047910
| NDC 9 | 53489-479 |
|---|---|
| NDC 10 | 53489-479-10 |
| NDC Item | 53489047910 |
| Packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-479-10) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 822189 |
| Imprint code | MP;116 |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 53489-479 |
NDC Item 55289093010
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-10 |
| NDC Item | 55289093010 |
| Packaging | 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093020
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-20 |
| NDC Item | 55289093020 |
| Packaging | 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55289093030
| NDC 9 | 55289-930 |
|---|---|
| NDC 10 | 55289-930-30 |
| NDC Item | 55289093030 |
| Packaging | 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 866003 |
| Imprint code | DAN;DAN;5660 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 55289-930 |
NDC Item 55700068260
| NDC 9 | 55700-682 |
|---|---|
| NDC 10 | 55700-682-60 |
| NDC Item | 55700068260 |
| Packaging | 60 TABLET in 1 BOTTLE (55700-682-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 385489 |
| Imprint code | E11 |
| Labeler | Quality Care Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2018-09-14 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 55700-682 |
NDC Item 61919021130
| NDC 9 | 61919-211 |
|---|---|
| NDC 10 | 61919-211-30 |
| NDC Item | 61919021130 |
| Packaging | 30 TABLET in 1 BOTTLE (61919-211-30) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 446580 |
| Imprint code | MP;116 |
| Labeler | Direct Rx |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-01-01 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 61919-211 |
NDC Item 61919074430
| NDC 9 | 61919-744 |
|---|---|
| NDC 10 | 61919-744-30 |
| NDC Item | 61919074430 |
| Related queries | Properties for NDC 9 61919-744 |
NDC Item 63629320801
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-1 |
| NDC Item | 63629320801 |
| Packaging | 30 TABLET in 1 BOTTLE (63629-3208-1) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 63629320802
| NDC 9 | 63629-3208 |
|---|---|
| NDC 10 | 63629-3208-2 |
| NDC Item | 63629320802 |
| Packaging | 60 TABLET in 1 BOTTLE (63629-3208-2) |
| ANDA | ANDA071795 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 611013 |
| Imprint code | DAN;DAN;5660 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 1990-04-03 |
| Marketing status | COMPLETED |
| Score | 2 |
| Shape | C48348 |
| Size | 11 mm |
| Related queries | Properties for NDC 9 63629-3208 |
NDC Item 66267019715
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-15 |
| NDC Item | 66267019715 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019720
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-20 |
| NDC Item | 66267019720 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019730
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-30 |
| NDC Item | 66267019730 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 66267019740
| NDC 9 | 66267-197 |
|---|---|
| NDC 10 | 66267-197-40 |
| NDC Item | 66267019740 |
| Related queries | Properties for NDC 9 66267-197 |
NDC Item 67544032853
| NDC 9 | 67544-328 |
|---|---|
| NDC 10 | 67544-328-53 |
| NDC Item | 67544032853 |
| Related queries | Properties for NDC 9 67544-328 |
NDC Item 67544041630
| NDC 9 | 67544-416 |
|---|---|
| NDC 10 | 67544-416-30 |
| NDC Item | 67544041630 |
| Related queries | Properties for NDC 9 67544-416 |
NDC Item 68387058860
| NDC 9 | 68387-588 |
|---|---|
| NDC 10 | 68387-588-60 |
| NDC Item | 68387058860 |
| Related queries | Properties for NDC 9 68387-588 |
NDC Item 71205064830
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-30 |
| NDC Item | 71205064830 |
| Packaging | 30 TABLET in 1 BOTTLE (71205-648-30) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064860
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-60 |
| NDC Item | 71205064860 |
| Packaging | 60 TABLET in 1 BOTTLE (71205-648-60) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 71205064890
| NDC 9 | 71205-648 |
|---|---|
| NDC 10 | 71205-648-90 |
| NDC Item | 71205064890 |
| Packaging | 90 TABLET in 1 BOTTLE (71205-648-90) |
| ANDA | ANDA072711 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 630116 |
| Imprint code | E11 |
| Labeler | Proficient Rx LP |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-25 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 14 mm |
| Related queries | Properties for NDC 9 71205-648 |
NDC Item 72789037401
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-01 |
| NDC Item | 72789037401 |
| Packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-374-01) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |
NDC Item 72789037482
| NDC 9 | 72789-374 |
|---|---|
| NDC 10 | 72789-374-82 |
| NDC Item | 72789037482 |
| Packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-374-82) |
| ANDA | ANDA072051 |
| COLORTEXT | yellow |
| Color | C48330 __ |
| FDA SPL set id | 868349 |
| Imprint code | MP;116 |
| Labeler | PD-Rx Pharmaceuticals, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-09-04 |
| Marketing status | ACTIVE |
| Score | 2 |
| Shape | C48348 |
| Size | 10 mm |
| Related queries | Properties for NDC 9 72789-374 |