Active Ingredient: TAMSULOSIN HYDROCHLORIDE
Proprietary Name: TAMSULOSIN HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A202010
Product Number: 001
Approval Date: Jan 4, 2013
Applicant Holder Full Name: ANCHEN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information