NDC properties for NDC 9 57664-327
NDC item 57664032706
NDC 9 | 57664-327 |
---|---|
NDC 10 | 57664-327-06 |
NDC Item | 57664032706 |
packaging | 60 TABLET, FILM COATED in 1 BOTTLE (57664-327-06) |
ANDA | ANDA075526 |
COLORTEXT | WHITE(white to off-white) |
Color | C48325 __ |
FDA SPL set id | 97406 |
Imprint code | 327 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2016-05-31 |
Marketing effective time low | 2002-09-26 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 15 mm |
NDC item 57664032713
NDC 9 | 57664-327 |
---|---|
NDC 10 | 57664-327-13 |
NDC Item | 57664032713 |
packaging | 500 TABLET, FILM COATED in 1 BOTTLE (57664-327-13) |
ANDA | ANDA075526 |
COLORTEXT | WHITE(white to off-white) |
Color | C48325 __ |
FDA SPL set id | 97406 |
Imprint code | 327 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2016-05-31 |
Marketing effective time low | 2002-09-26 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 15 mm |
NDC item 57664032783
NDC 9 | 57664-327 |
---|---|
NDC 10 | 57664-327-83 |
NDC Item | 57664032783 |
packaging | 30 TABLET, FILM COATED in 1 BOTTLE (57664-327-83) |
ANDA | ANDA075526 |
COLORTEXT | WHITE(white to off-white) |
Color | C48325 __ |
FDA SPL set id | 97406 |
Imprint code | 327 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2016-05-31 |
Marketing effective time low | 2002-09-26 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 15 mm |
NDC item 57664032786
NDC 9 | 57664-327 |
---|---|
NDC 10 | 57664-327-86 |
NDC Item | 57664032786 |
packaging | 60 TABLET, FILM COATED in 1 BOTTLE (57664-327-86) |
ANDA | ANDA075526 |
COLORTEXT | WHITE(white to off-white) |
Color | C48325 __ |
FDA SPL set id | 97406 |
Imprint code | 327 |
Labeler | Sun Pharmaceutical Industries, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2016-05-31 |
Marketing effective time low | 2002-09-26 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 15 mm |
NDC item 60505002702
NDC 9 | 60505-0027 |
---|---|
NDC 10 | 60505-0027-2 |
NDC Item | 60505002702 |
packaging | 30 TABLET, FILM COATED in 1 BOTTLE (60505-0027-2) |
ANDA | ANDA075089 |
COLORTEXT | WHITE |
Color | C48325 __ |
FDA SPL set id | 266137 |
Imprint code | APO;027 |
Labeler | Apotex Corp. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2012-04-30 |
Marketing effective time low | 1999-07-01 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 14 mm |
NDC item 60505002704
NDC 9 | 60505-0027 |
---|---|
NDC 10 | 60505-0027-4 |
NDC Item | 60505002704 |
packaging | 60 TABLET, FILM COATED in 1 BOTTLE (60505-0027-4) |
ANDA | ANDA075089 |
COLORTEXT | WHITE |
Color | C48325 __ |
FDA SPL set id | 266137 |
Imprint code | APO;027 |
Labeler | Apotex Corp. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2012-04-30 |
Marketing effective time low | 1999-07-01 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 14 mm |
NDC item 60505002707
NDC 9 | 60505-0027 |
---|---|
NDC 10 | 60505-0027-7 |
NDC Item | 60505002707 |
packaging | 500 TABLET, FILM COATED in 1 BOTTLE (60505-0027-7) |
ANDA | ANDA075089 |
COLORTEXT | WHITE |
Color | C48325 __ |
FDA SPL set id | 266137 |
Imprint code | APO;027 |
Labeler | Apotex Corp. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2012-04-30 |
Marketing effective time low | 1999-07-01 |
Marketing status | COMPLETED |
Score | 1 |
Shape | C48345 |
Size | 14 mm |