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:
Application Number: A079014
Product Number: 001
Approval Date: Jul 18, 2011
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information