# Venlafaxine

NDC: 57664-396
Generic name: Venlafaxine
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080613

FDA application: ANDA078627

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-396"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-396
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55889b3d-74c9-4638-9a14-6a4ca3a99f7f