# Venlafaxine Hydrochloride

NDC: 0093-7385
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20100701

FDA application: ANDA076565

## 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:"0093-7385"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7385
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9a30e1b5-272b-4109-ad6c-a3c9a895822f