Active Ingredient: SUPROFEN
Proprietary Name: PROFENAL
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019387
Product Number: 001
Approval Date: Dec 23, 1988
Applicant Holder Full Name: ALCON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
