Active Ingredient: ANASTROZOLE
Proprietary Name: ANASTROZOLE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078921
Product Number: 001
Approval Date: Jun 28, 2010
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information