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: A074615
Product Number: 001
Approval Date: Sep 29, 1995
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information