# Venlafaxine

NDC: 70771-1652
Generic name: Venlafaxine
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220901

FDA application: ANDA215622

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1652"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1652
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=750333ce-a512-42e1-b9e3-179714b488df