# Venlafaxine Hydrochloride

NDC: 70710-1698
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230518

FDA application: ANDA090174

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1698"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1698
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9fda0f8d-b24e-4581-9dca-7aaaf86e2413