Active Ingredient: BRIMONIDINE TARTRATE
Proprietary Name: LUMIFY PRESERVATIVE FREE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.025%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N218424
Product Number: 001
Approval Date: Apr 19, 2024
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
