NDC properties for NDC 9 0378-0427
NDC item 00378042701
NDC 9 | 0378-0427 |
---|---|
NDC 10 | 0378-0427-01 |
NDC Item | 00378042701 |
packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0427-01) |
ANDA | ANDA073039 |
COLORTEXT | YELLOW(yellow-orange) |
Color | C48330 __ |
FDA SPL set id | 571333 |
Imprint code | MYLAN;427 |
Labeler | Mylan Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2021-07-31 |
Marketing effective time low | 1993-06-22 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48348 |
Size | 10 mm |
NDC item 00591566101
NDC 9 | 0591-5661 |
---|---|
NDC 10 | 0591-5661-01 |
NDC Item | 00591566101 |
packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5661-01) |
ANDA | ANDA071891 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 838697 |
Imprint code | DAN;5661 |
Labeler | Actavis Pharma, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1990-04-03 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 10 mm |
NDC item 00591566105
NDC 9 | 0591-5661 |
---|---|
NDC 10 | 0591-5661-05 |
NDC Item | 00591566105 |
packaging | 500 TABLET in 1 BOTTLE, PLASTIC (0591-5661-05) |
ANDA | ANDA071891 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 838697 |
Imprint code | DAN;5661 |
Labeler | Actavis Pharma, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1990-04-03 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 10 mm |
NDC item 00904733460
NDC 9 | 0904-7334 |
---|---|
NDC 10 | 0904-7334-60 |
NDC Item | 00904733460 |
packaging | 100 TABLET in 1 BOTTLE, PLASTIC (0904-7334-60) |
ANDA | ANDA072050 |
COLORTEXT | YELLOW |
Color | C48330 __ |
FDA SPL set id | 862124 |
Imprint code | MP;112 |
Labeler | Major Pharmaceuticals |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-07-27 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 23155000501
NDC 9 | 23155-005 |
---|---|
NDC 10 | 23155-005-01 |
NDC Item | 23155000501 |
packaging | 100 TABLET in 1 BOTTLE (23155-005-01) |
ANDA | ANDA073262 |
COLORTEXT | YELLOW(bright yellow) |
Color | C48330 __ |
FDA SPL set id | 73663 |
Imprint code | HP;5 |
Labeler | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2007-07-16 |
Marketing status | COMPLETED |
Score | 2 |
Shapetext | convex |
Shape | C48348 |
Size | 10 mm |
NDC item 24658077001
NDC 9 | 24658-770 |
---|---|
NDC 10 | 24658-770-01 |
NDC Item | 24658077001 |
packaging | 100 TABLET in 1 BOTTLE (24658-770-01) |
ANDA | ANDA072710 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 756082 |
Imprint code | E10 |
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 | 10 mm |
NDC item 24658077005
NDC 9 | 24658-770 |
---|---|
NDC 10 | 24658-770-05 |
NDC Item | 24658077005 |
packaging | 500 TABLET in 1 BOTTLE (24658-770-05) |
ANDA | ANDA072710 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 756082 |
Imprint code | E10 |
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 | 10 mm |
NDC item 42806001801
NDC 9 | 42806-018 |
---|---|
NDC 10 | 42806-018-01 |
NDC Item | 42806001801 |
packaging | 100 TABLET in 1 BOTTLE (42806-018-01) |
ANDA | ANDA072710 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 844548 |
Imprint code | E10 |
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 | 10 mm |
NDC item 42806001805
NDC 9 | 42806-018 |
---|---|
NDC 10 | 42806-018-05 |
NDC Item | 42806001805 |
packaging | 500 TABLET in 1 BOTTLE (42806-018-05) |
ANDA | ANDA072710 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 844548 |
Imprint code | E10 |
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 | 10 mm |
NDC item 42806001810
NDC 9 | 42806-018 |
---|---|
NDC 10 | 42806-018-10 |
NDC Item | 42806001810 |
packaging | 1000 TABLET in 1 BOTTLE (42806-018-10) |
ANDA | ANDA072710 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 844548 |
Imprint code | E10 |
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 | 10 mm |
NDC item 52959019600
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-00 |
NDC Item | 52959019600 |
NDC item 52959019610
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-10 |
NDC Item | 52959019610 |
NDC item 52959019614
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-14 |
NDC Item | 52959019614 |
NDC item 52959019615
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-15 |
NDC Item | 52959019615 |
NDC item 52959019620
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-20 |
NDC Item | 52959019620 |
NDC item 52959019630
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-30 |
NDC Item | 52959019630 |
NDC item 52959019660
NDC 9 | 52959-196 |
---|---|
NDC 10 | 52959-196-60 |
NDC Item | 52959019660 |
NDC item 53489047801
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-01 |
NDC Item | 53489047801 |
packaging | 100 TABLET in 1 BOTTLE, PLASTIC (53489-478-01) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 53489047802
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-02 |
NDC Item | 53489047802 |
packaging | 50 TABLET in 1 BOTTLE, PLASTIC (53489-478-02) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 53489047803
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-03 |
NDC Item | 53489047803 |
packaging | 250 TABLET in 1 BOTTLE, PLASTIC (53489-478-03) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 53489047805
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-05 |
NDC Item | 53489047805 |
packaging | 500 TABLET in 1 BOTTLE, PLASTIC (53489-478-05) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 53489047806
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-06 |
NDC Item | 53489047806 |
packaging | 60 TABLET in 1 BOTTLE, PLASTIC (53489-478-06) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 53489047810
NDC 9 | 53489-478 |
---|---|
NDC 10 | 53489-478-10 |
NDC Item | 53489047810 |
packaging | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-478-10) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 822189 |
Imprint code | MP;112 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 55289054130
NDC 9 | 55289-541 |
---|---|
NDC 10 | 55289-541-30 |
NDC Item | 55289054130 |
NDC item 63629496501
NDC 9 | 63629-4965 |
---|---|
NDC 10 | 63629-4965-1 |
NDC Item | 63629496501 |
packaging | 150 TABLET in 1 BOTTLE (63629-4965-1) |
ANDA | ANDA071891 |
COLORTEXT | YELLOW |
Color | C48330 __ |
FDA SPL set id | 126122 |
Imprint code | DAN;5661 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1990-04-03 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48348 |
Size | 10 mm |
NDC item 63629496502
NDC 9 | 63629-4965 |
---|---|
NDC 10 | 63629-4965-2 |
NDC Item | 63629496502 |
packaging | 60 TABLET in 1 BOTTLE (63629-4965-2) |
ANDA | ANDA071891 |
COLORTEXT | YELLOW |
Color | C48330 __ |
FDA SPL set id | 126122 |
Imprint code | DAN;5661 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1990-04-03 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48348 |
Size | 10 mm |
NDC item 66267026420
NDC 9 | 66267-264 |
---|---|
NDC 10 | 66267-264-20 |
NDC Item | 66267026420 |
NDC item 72789037301
NDC 9 | 72789-373 |
---|---|
NDC 10 | 72789-373-01 |
NDC Item | 72789037301 |
packaging | 100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 868883 |
Imprint code | MP;112 |
Labeler | PD-Rx Pharmaceuticals, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |
NDC item 72789037382
NDC 9 | 72789-373 |
---|---|
NDC 10 | 72789-373-82 |
NDC Item | 72789037382 |
packaging | 500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82) |
ANDA | ANDA072050 |
COLORTEXT | yellow |
Color | C48330 __ |
FDA SPL set id | 868883 |
Imprint code | MP;112 |
Labeler | PD-Rx Pharmaceuticals, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-09-04 |
Marketing status | ACTIVE |
Score | 1 |
Shape | C48348 |
Size | 9 mm |