| 50090-4853-0 |
50090-4853 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200120 |
N/A |
ANDA |
ANDA090555 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE (50090-4853-0) |
| 50090-4853-1 |
50090-4853 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200120 |
N/A |
ANDA |
ANDA090555 |
A-S Medication Solutions |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE (50090-4853-1) |
| 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) |
| 57237-173-90 |
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 |
90 TABLET in 1 BOTTLE (57237-173-90) |
| 71335-1104-1 |
71335-1104 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20190220 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
60 TABLET in 1 BOTTLE (71335-1104-1) |
| 71335-1104-2 |
71335-1104 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20190213 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE (71335-1104-2) |
| 71335-1104-3 |
71335-1104 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200103 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (71335-1104-3) |
| 71335-1104-4 |
71335-1104 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20211228 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
28 TABLET in 1 BOTTLE (71335-1104-4) |
| 71335-1104-5 |
71335-1104 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20211228 |
N/A |
ANDA |
ANDA090555 |
Bryant Ranch Prepack |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
120 TABLET in 1 BOTTLE (71335-1104-5) |
| 65862-405-01 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET in 1 BOTTLE (65862-405-01) |
| 65862-405-10 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-405-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-405-30 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE (65862-405-30) |
| 65862-405-60 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE (65862-405-60) |
| 65862-405-66 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
6000 TABLET in 1 BOTTLE (65862-405-66) |
| 65862-405-90 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE (65862-405-90) |
| 65862-405-99 |
65862-405 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
1000 TABLET in 1 BOTTLE (65862-405-99) |
| 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) |
| 70518-1385-0 |
70518-1385 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20180824 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-1385-0) |
| 70518-1385-1 |
70518-1385 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20181004 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1) |