Active Ingredient: BRINZOLAMIDE
Proprietary Name: BRINZOLAMIDE
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204884
Product Number: 001
Approval Date: Aug 18, 2021
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information
