68180-645-06 |
68180-645 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
PAROXETINE |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170306 |
N/A |
ANDA |
ANDA204134 |
Lupin Pharmaceuticals, Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
37.5 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-645-06) |
68180-646-06 |
68180-646 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
PAROXETINE |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20170306 |
N/A |
ANDA |
ANDA204134 |
Lupin Pharmaceuticals, Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
25 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-646-06) |
70518-3613-0 |
70518-3613 |
HUMAN PRESCRIPTION DRUG |
PAROXETINE |
PAROXETINE |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20230109 |
N/A |
ANDA |
ANDA204134 |
REMEDYREPACK INC. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
25 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3613-0) |