Active Ingredient: OFLOXACIN
Proprietary Name: OCUFLOX
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.3%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AT
Application Number: N019921
Product Number: 001
Approval Date: Jul 30, 1993
Applicant Holder Full Name: ALLERGAN INC
Marketing Status:
Prescription
Patent and Exclusivity Information