| 65862-407-90 |
65862-407 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (65862-407-90) |
| 65862-407-99 |
65862-407 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
1000 TABLET in 1 BOTTLE (65862-407-99) |
| 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) |
| 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) |
| 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) |
| 65862-408-01 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
100 TABLET in 1 BOTTLE (65862-408-01) |
| 65862-408-10 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
10 BLISTER PACK in 1 CARTON (65862-408-10) / 10 TABLET in 1 BLISTER PACK |
| 65862-408-20 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
20 TABLET in 1 BOTTLE (65862-408-20) |
| 65862-408-66 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
6000 TABLET in 1 BOTTLE (65862-408-66) |
| 65862-408-90 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
90 TABLET in 1 BOTTLE (65862-408-90) |
| 65862-408-99 |
65862-408 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine |
Venlafaxine Hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Aurobindo Pharma Limited |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
1000 TABLET in 1 BOTTLE (65862-408-99) |
| 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) |
| 51655-223-26 |
51655-223 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20230227 |
N/A |
ANDA |
ANDA090555 |
Northwind Health Company, LLC |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE, PLASTIC (51655-223-26) |
| 51655-223-52 |
51655-223 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20221025 |
N/A |
ANDA |
ANDA090555 |
Northwind Health Company, LLC |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (51655-223-52) |
| 51655-323-52 |
51655-323 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20230502 |
N/A |
ANDA |
ANDA090555 |
Northwind Health Company, LLC |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52) |
| 60760-187-60 |
60760-187 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20190529 |
N/A |
ANDA |
ANDA090555 |
St. Mary's Medical Park Pharmacy |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE, PLASTIC (60760-187-60) |
| 60760-304-30 |
60760-304 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200616 |
N/A |
ANDA |
ANDA090555 |
St. Mary's Medical Park Pharmacy |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (60760-304-30) |
| 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) |