47335-794-08 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08) |
47335-794-13 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13) |
47335-794-81 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190815 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81) |
47335-794-83 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83) |
47335-794-88 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88) |
47335-794-99 |
47335-794 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
225 mg/1 |
5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
47335-758-08 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-08) |
47335-758-18 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-18) |
47335-758-81 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-81) |
47335-758-83 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-83) |
47335-758-88 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-88) |
47335-758-99 |
47335-758 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190329 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
150 mg/1 |
2 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-758-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
47335-760-08 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-08) |
47335-760-18 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-18) |
47335-760-61 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190329 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
10 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-760-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
47335-760-81 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-81) |
47335-760-83 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-83) |
47335-760-88 |
47335-760 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
37.5 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-760-88) |
47335-759-08 |
47335-759 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-08) |
47335-759-18 |
47335-759 |
HUMAN PRESCRIPTION DRUG |
Venlafaxine Hydrochloride |
Venlafaxine Hydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20141215 |
N/A |
ANDA |
ANDA091272 |
Sun Pharmaceutical Industries, Inc. |
VENLAFAXINE HYDROCHLORIDE |
75 mg/1 |
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-759-18) |