# Venlafaxine

NDC: 71610-606
Generic name: Venlafaxine
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
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: 75 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-606"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-606
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2887a463-2da1-4f8d-afef-f4c88d31e04d
