# Alfuzosin Hydrochloride

NDC: 71335-2146
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: 20111122

FDA application: ANDA079057

## 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:"71335-2146"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2146
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98fa10c2-7c12-44aa-9112-e2fd6fa71d06