# Alfuzosin hydrochloride

NDC: 76282-302
Generic name: Alfuzosin hydrochloride
Labeler / Manufacturer: Exelan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20121002

FDA application: ANDA090284

## 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:"76282-302"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-302
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f075a897-7bef-4799-b7e2-7e051c461443