Active Ingredient: LATANOPROST
Proprietary Name: LATANOPROST
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.005%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206519
Product Number: 001
Approval Date: Sep 3, 2019
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information