Drug application
VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE)
Drugs@FDA ANDA 091272 · SUN PHARM
Key facts
| Drug name | VENLAFAXINE HYDROCHLORIDE |
|---|---|
| Active ingredients | VENLAFAXINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 091272 |
| Company | SUN PHARM |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | EQ 37.5MG BASE |
| Marketing status | Discontinued |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Aug 18, 2010 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.