| 70518-1385-3 |
70518-1385 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20231107 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
60 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3) |
| 70518-1976-0 |
70518-1976 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20190325 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
100 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-1976-0) |
| 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) |
| 70518-2652-1 |
70518-2652 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200327 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-2652-1) |
| 70518-2652-2 |
70518-2652 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20201223 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
30 TABLET in 1 BOTTLE, PLASTIC (70518-2652-2) |
| 70518-2659-0 |
70518-2659 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20200327 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
25 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-2659-0) |
| 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) |
| 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) |
| 70518-1907-0 |
70518-1907 |
HUMAN PRESCRIPTION DRUG |
venlafaxine |
venlafaxine hydrochloride |
TABLET |
ORAL |
20190225 |
N/A |
ANDA |
ANDA090555 |
REMEDYREPACK INC. |
VENLAFAXINE HYDROCHLORIDE |
50 mg/1 |
30 TABLET in 1 BLISTER PACK (70518-1907-0) |
| 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) |
| 57237-172-01 |
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) |
| 57237-174-90 |
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) |
| 57237-176-90 |
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) |
| 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) |
| 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) |