Active Ingredient: LIFITEGRAST
Proprietary Name: LIFITEGRAST
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 5%
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A215081
Product Number: 001
Approval Date: Aug 4, 2023
Applicant Holder Full Name: MICRO LABS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information