# Alfuzosin Hydrochloride

NDC: 51655-087
Generic name: Alfuzosin Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20221004

FDA application: ANDA079060

## Active ingredients

- ALFUZOSIN HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-087"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-087
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2a530bd-6a86-251d-e053-2995a90adac4