# Venlafaxine Hydrochloride

NDC: 47335-760
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20141215

FDA application: ANDA091272

## 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:"47335-760"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-760
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc989aa7-c4ab-4359-a971-523eb477ef9b