Active Ingredient: ALFUZOSIN HYDROCHLORIDE
Proprietary Name: UROXATRAL
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N021287
Product Number: 001
Approval Date: Jun 12, 2003
Applicant Holder Full Name: CONCORDIA PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
