# Venlafaxine

NDC: 71335-2709
Generic name: Venlafaxine
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080613

FDA application: ANDA077653

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4638a83-2720-430c-b529-c852aa2f7366