Active Ingredient: LATANOPROST; NETARSUDIL DIMESYLATE
Proprietary Name: ROCKLATAN
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.005%;EQ 0.02% BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N208259
Product Number: 001
Approval Date: Mar 12, 2019
Applicant Holder Full Name: ALCON LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
