# VENLAFAXINE HYDROCHLORIDE
> **ANDA091272** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM · Approved 2010-08-18
## Drug
- **FDA Application Number:** ANDA091272
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** VENLAFAXINE HYDROCHLORIDE
- **Generic name:** VENLAFAXINE HYDROCHLORIDE
- **Active ingredients:** VENLAFAXINE HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** SUN PHARM
- **Manufacturer:** Sun Pharmaceutical Industries, Inc.
- **First approval:** 2010-08-18
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=091272)
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