Drug application
VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE)
Drugs@FDA ANDA 200834 · AUROBINDO PHARMA LTD
Key facts
| Drug name | VENLAFAXINE HYDROCHLORIDE |
|---|---|
| Active ingredients | VENLAFAXINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 200834 |
| Company | AUROBINDO PHARMA LTD |
| Dosage forms | CAPSULE, EXTENDED RELEASE, ORAL |
| Strength | EQ 37.5MG BASE |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission class | Not Applicable |
| Latest submission status date | Apr 14, 2011 |
At a glance
- 1–9 Submissions
- 10–99 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.