Active Ingredient: SULINDAC
Proprietary Name: SULINDAC
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072712
Product Number: 001
Approval Date: Aug 30, 1991
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
