Active Ingredient: DICLOFENAC SODIUM
Proprietary Name: DICLOFENAC SODIUM
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.1%
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AT
Application Number: A078792
Product Number: 001
Approval Date: Dec 28, 2007
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information