# Alfuzosin hydrochloride

NDC: 63629-9155
Generic name: Alfuzosin hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160315

FDA application: ANDA203192

## Active ingredients

- ALFUZOSIN HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-9155"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-9155
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c01d4d6b-e030-4b8f-aaa9-4df0f3f8fbda