| 68382-019-10 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
1000 TABLET in 1 BOTTLE (68382-019-10) |
| 68382-019-14 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE (68382-019-14) |
| 68382-019-16 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE (68382-019-16) |
| 68382-020-01 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
100 TABLET in 1 BOTTLE (68382-020-01) |
| 68382-020-05 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
500 TABLET in 1 BOTTLE (68382-020-05) |
| 68382-020-06 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
30 TABLET in 1 BOTTLE (68382-020-06) |
| 68382-020-10 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
1000 TABLET in 1 BOTTLE (68382-020-10) |
| 68382-020-14 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
60 TABLET in 1 BOTTLE (68382-020-14) |
| 68382-020-16 |
68382-020 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
90 TABLET in 1 BOTTLE (68382-020-16) |
| 68382-021-01 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
100 TABLET in 1 BOTTLE (68382-021-01) |
| 68382-021-05 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
500 TABLET in 1 BOTTLE (68382-021-05) |
| 68382-021-06 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE (68382-021-06) |
| 68382-021-10 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
1000 TABLET in 1 BOTTLE (68382-021-10) |
| 68382-021-14 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
60 TABLET in 1 BOTTLE (68382-021-14) |
| 68382-021-16 |
68382-021 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (68382-021-16) |
| 50090-4865-0 |
50090-4865 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20200123 |
N/A |
ANDA |
ANDA077653 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE (50090-4865-0) |
| 50090-4865-1 |
50090-4865 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20200123 |
N/A |
ANDA |
ANDA077653 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE (50090-4865-1) |
| 60760-121-30 |
60760-121 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20110130 |
N/A |
ANDA |
ANDA077653 |
St. Marys Medical Park Pharmacy |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (60760-121-30) |
| 60760-728-60 |
60760-728 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20230421 |
N/A |
ANDA |
ANDA077653 |
ST. MARY'S MEDICAL PARK PHARMACY |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60) |
| 68382-101-01 |
68382-101 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
100 TABLET in 1 BOTTLE (68382-101-01) |