| 65841-675-01 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
100 TABLET in 1 BOTTLE (65841-675-01) |
| 65841-675-05 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
500 TABLET in 1 BOTTLE (65841-675-05) |
| 65841-675-06 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
30 TABLET in 1 BOTTLE (65841-675-06) |
| 65841-675-10 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
1000 TABLET in 1 BOTTLE (65841-675-10) |
| 65841-675-14 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
60 TABLET in 1 BOTTLE (65841-675-14) |
| 65841-675-16 |
65841-675 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Lifesciences Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
90 TABLET in 1 BOTTLE (65841-675-16) |
| 50090-2408-0 |
50090-2408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20160519 |
N/A |
ANDA |
ANDA077653 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE (50090-2408-0) |
| 50090-2408-1 |
50090-2408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20160519 |
N/A |
ANDA |
ANDA077653 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (50090-2408-1) |
| 68071-2990-9 |
68071-2990 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20230424 |
N/A |
ANDA |
ANDA077653 |
NuCare Pharmaceuticals,Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (68071-2990-9) |
| 68071-3431-0 |
68071-3431 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20230727 |
N/A |
ANDA |
ANDA077653 |
NuCare Pharmaceuticals,Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET in 1 BOTTLE (68071-3431-0) |
| 68071-3432-0 |
68071-3432 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20230619 |
N/A |
ANDA |
ANDA077653 |
NuCare Pharmaceuticals,Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
100 TABLET in 1 BOTTLE (68071-3432-0) |
| 68382-018-01 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
100 TABLET in 1 BOTTLE (68382-018-01) |
| 68382-018-05 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
500 TABLET in 1 BOTTLE (68382-018-05) |
| 68382-018-06 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
30 TABLET in 1 BOTTLE (68382-018-06) |
| 68382-018-10 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
1000 TABLET in 1 BOTTLE (68382-018-10) |
| 68382-018-14 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
60 TABLET in 1 BOTTLE (68382-018-14) |
| 68382-018-16 |
68382-018 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
90 TABLET in 1 BOTTLE (68382-018-16) |
| 68382-019-01 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET in 1 BOTTLE (68382-019-01) |
| 68382-019-05 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
500 TABLET in 1 BOTTLE (68382-019-05) |
| 68382-019-06 |
68382-019 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE (68382-019-06) |