Active Ingredient: GEMFIBROZIL
Proprietary Name: GEMFIBROZIL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A079239
Product Number: 001
Approval Date: Dec 29, 2008
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
