# Venlafaxine Hydrochloride

NDC: 0615-8346
Generic name: Venlafaxine Hydrochloride
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
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: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3eef522f-9e95-4668-bb12-09fd47ed0daf