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) |
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) |
57237-173-01 |
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) |
57237-174-01 |
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) |
57237-175-01 |
57237-175 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
100 TABLET in 1 BOTTLE (57237-175-01) |
57237-175-90 |
57237-175 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20100407 |
N/A |
ANDA |
ANDA090555 |
Rising Pharma Holdings, Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (57237-175-90) |
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) |
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) |
51655-223-26 |
51655-223 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20230227 |
N/A |
ANDA |
ANDA090555 |
Northwind Pharmaceuticals, 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 Pharmaceuticals, 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 Pharmaceuticals, LLC |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52) |
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) |
55700-816-90 |
55700-816 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20191108 |
N/A |
ANDA |
ANDA090555 |
Quality Care Products, LLC |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
90 TABLET in 1 BOTTLE (55700-816-90) |
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) |