# Venlafaxine Hydrochloride

NDC: 82804-038
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20111123

FDA application: ANDA200834

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-038"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-038
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c558ab8-b4b3-4973-b016-ed5cfcb4d88b