Active Ingredient: TRAVOPROST
Proprietary Name: TRAVOPROST
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.004%
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A203431
Product Number: 001
Approval Date: Jul 10, 2015
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Prescription
Patent and Exclusivity Information
