Active Ingredient: TRIFLURIDINE
Proprietary Name: TRIFLURIDINE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A205438
Product Number: 001
Approval Date: Jul 28, 2017
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
