Active Ingredient: ALFUZOSIN HYDROCHLORIDE
Proprietary Name: ALFUZOSIN HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079057
Product Number: 001
Approval Date: Jul 18, 2011
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
