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: A077697
Product Number: 001
Approval Date: Mar 22, 2011
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
