Active Ingredient: FLURBIPROFEN SODIUM
Proprietary Name: FLURBIPROFEN SODIUM
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.03%
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A074447
Product Number: 001
Approval Date: Jan 4, 1995
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information