# Venlafaxine Hydrochloride

NDC: 65841-673
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080613

FDA application: ANDA077653

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65841-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51334651-7a7f-4653-bf9d-d5be04fd902d