Active Ingredient: FLURBIPROFEN SODIUM
Proprietary Name: OCUFEN
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.03% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019404
Product Number: 001
Approval Date: Dec 31, 1986
Applicant Holder Full Name: ALLERGAN PHARMACEUTICAL
Marketing Status:
Discontinued
Patent and Exclusivity Information