Active Ingredient: OFLOXACIN
Proprietary Name: OFLOXACIN
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.3%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076231
Product Number: 001
Approval Date: May 14, 2004
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Discontinued
Patent and Exclusivity Information