# Venlafaxine Hydrochloride

NDC: 42806-601
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20220907

FDA application: ANDA214654

## 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:"42806-601"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-601
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=430777f0-347c-4f21-8c5d-55f4e9897e74