# Venlafaxine Hydrochloride

NDC: 71335-1864
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20110601

FDA application: ANDA200834

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-1864"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1864
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bff505db-2752-41fc-a4dd-4773f629106e