Active Ingredient: LEUPROLIDE ACETATE
Proprietary Name: LEUPROLIDE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1MG/0.2ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A078885
Product Number: 001
Approval Date: Mar 9, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information