# venlafaxine

NDC: 62332-009
Generic name: venlafaxine
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151001

FDA application: ANDA078932

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=67b323a7-a8c9-410f-bff0-0e515bef41a7