# Venlafaxine Hydrochloride

NDC: 69367-418
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20251118

FDA application: ANDA205468

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 225 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-418"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-418
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=349308ef-2caf-4fec-b428-56ae06c6771d