68788-6870-9 |
68788-6870 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20170111 |
N/A |
ANDA |
ANDA077584 |
Preferred Pharmaceuticals Inc. |
PAROXETINE HYDROCHLORIDE |
40 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68788-6870-9) |
68382-097-01 |
68382-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (68382-097-01) |
68382-097-05 |
68382-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
10 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (68382-097-05) |
68382-097-06 |
68382-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68382-097-06) |
68382-097-10 |
68382-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
10 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (68382-097-10) |
68382-097-16 |
68382-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
10 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68382-097-16) |
68382-098-01 |
68382-098 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
20 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (68382-098-01) |
68382-098-05 |
68382-098 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
20 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (68382-098-05) |
68382-098-06 |
68382-098 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
20 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68382-098-06) |
68382-098-10 |
68382-098 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
20 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (68382-098-10) |
68382-098-16 |
68382-098 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
20 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68382-098-16) |
68382-099-01 |
68382-099 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
30 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (68382-099-01) |
68382-099-05 |
68382-099 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
30 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (68382-099-05) |
68382-099-06 |
68382-099 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
30 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68382-099-06) |
68382-099-10 |
68382-099 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
30 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (68382-099-10) |
68382-099-16 |
68382-099 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Pharmaceuticals USA Inc. |
PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
30 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (68382-099-16) |
65841-097-01 |
65841-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Lifesciences Limited |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (65841-097-01) |
65841-097-05 |
65841-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Lifesciences Limited |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE (65841-097-05) |
65841-097-06 |
65841-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Lifesciences Limited |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (65841-097-06) |
65841-097-10 |
65841-097 |
HUMAN PRESCRIPTION DRUG |
Paroxetine |
Paroxetine Hydrochloride |
TABLET, FILM COATED |
ORAL |
20070413 |
N/A |
ANDA |
ANDA077584 |
Zydus Lifesciences Limited |
PAROXETINE HYDROCHLORIDE ANHYDROUS |
10 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (65841-097-10) |