# Venlafaxine

NDC: 68071-3432
Generic name: Venlafaxine
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20080613

FDA application: ANDA077653

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-3432"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3432
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe7de51e-8a81-fe68-e053-6294a90a7339