Active Ingredient: BROMFENAC SODIUM
Proprietary Name: BROMSITE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.075% ACID
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N206911
Product Number: 001
Approval Date: Apr 8, 2016
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information