| 68382-101-06 |
68382-101 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
30 TABLET in 1 BOTTLE (68382-101-06) |
| 68382-101-10 |
68382-101 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
1000 TABLET in 1 BOTTLE (68382-101-10) |
| 68382-101-14 |
68382-101 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
60 TABLET in 1 BOTTLE (68382-101-14) |
| 68382-101-16 |
68382-101 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20080613 |
N/A |
ANDA |
ANDA077653 |
Zydus Pharmaceuticals USA Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
90 TABLET in 1 BOTTLE (68382-101-16) |
| 63187-414-30 |
63187-414 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20190101 |
N/A |
ANDA |
ANDA077653 |
Proficient Rx LP |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE (63187-414-30) |
| 63187-414-60 |
63187-414 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20190101 |
N/A |
ANDA |
ANDA077653 |
Proficient Rx LP |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
60 TABLET in 1 BOTTLE (63187-414-60) |
| 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) |
| 71335-2709-1 |
71335-2709 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20250926 |
N/A |
ANDA |
ANDA077653 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
30 TABLET in 1 BOTTLE (71335-2709-1) |
| 71335-2709-2 |
71335-2709 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20250926 |
N/A |
ANDA |
ANDA077653 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
60 TABLET in 1 BOTTLE (71335-2709-2) |
| 71335-2709-3 |
71335-2709 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20250926 |
N/A |
ANDA |
ANDA077653 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
90 TABLET in 1 BOTTLE (71335-2709-3) |
| 71335-2709-4 |
71335-2709 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20250926 |
N/A |
ANDA |
ANDA077653 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
18 TABLET in 1 BOTTLE (71335-2709-4) |
| 68001-159-00 |
68001-159 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine |
TABLET |
ORAL |
20131125 |
N/A |
ANDA |
ANDA077653 |
BluePoint Laboratories |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
100 TABLET in 1 BOTTLE (68001-159-00) |
| 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) |
| 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) |
| 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) |
| 68382-019-05 |
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) |