# venlafaxine

NDC: 50090-4853
Generic name: venlafaxine hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100407

FDA application: ANDA090555

## Active ingredients

- VENLAFAXINE HYDROCHLORIDE: 37.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-4853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-4853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5bd03cf1-e8fc-44f3-9c41-06515b897f3b