| 65862-406-01 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
100 TABLET in 1 BOTTLE (65862-406-01) |
| 65862-406-10 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-406-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-406-30 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
30 TABLET in 1 BOTTLE (65862-406-30) |
| 65862-406-59 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
5000 TABLET in 1 BOTTLE (65862-406-59) |
| 65862-406-90 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
90 TABLET in 1 BOTTLE (65862-406-90) |
| 65862-406-99 |
65862-406 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
1000 TABLET in 1 BOTTLE (65862-406-99) |
| 57237-173-01 |
57237-173 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET in 1 BOTTLE (57237-173-01) |
| 71335-1213-1 |
71335-1213 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20220209 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE (71335-1213-1) |
| 71335-1213-2 |
71335-1213 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20220209 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE (71335-1213-2) |
| 71335-1213-3 |
71335-1213 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20220209 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE (71335-1213-3) |
| 71335-1213-4 |
71335-1213 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20220209 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
10 TABLET in 1 BOTTLE (71335-1213-4) |
| 57237-172-01 |
57237-172 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
100 TABLET in 1 BOTTLE (57237-172-01) |
| 57237-172-90 |
57237-172 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
90 TABLET in 1 BOTTLE (57237-172-90) |
| 57237-176-01 |
57237-176 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
100 TABLET in 1 BOTTLE (57237-176-01) |
| 57237-176-90 |
57237-176 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
90 TABLET in 1 BOTTLE (57237-176-90) |
| 70518-2652-0 |
70518-2652 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200325 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE, PLASTIC (70518-2652-0) |
| 57237-174-01 |
57237-174 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
100 TABLET in 1 BOTTLE (57237-174-01) |
| 57237-174-90 |
57237-174 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
90 TABLET in 1 BOTTLE (57237-174-90) |
| 65862-404-01 |
65862-404 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
100 TABLET in 1 BOTTLE (65862-404-01) |
| 65862-404-10 |
65862-404 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-404-10) / 10 TABLET in 1 BLISTER PACK |