# Venlafaxine Hydrochloride

NDC: 31722-002
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190708

FDA application: ANDA212277

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0ee91447-2c23-4519-81cc-550b5416dd6b