# Venlafaxine Hydrochloride

NDC: 0093-9149
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20060804

FDA application: ANDA076690

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-9149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-9149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=37aaa8ac-4e0c-4e04-98b5-19b0d90d857c