# Alfuzosin Hydrochloride

NDC: 47335-956
Generic name: Alfuzosin Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
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:"47335-956"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-956
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2af616e-673a-4fdd-ace8-db2d0f154604