Active Ingredient: LATANOPROSTENE BUNOD
Proprietary Name: VYZULTA
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.024%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N207795
Product Number: 001
Approval Date: Nov 2, 2017
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information
