Active Ingredient: BIMATOPROST
Proprietary Name: BIMATOPROST
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.03%
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A205537
Product Number: 001
Approval Date: Oct 6, 2022
Applicant Holder Full Name: EUGIA PHARMA SPECIALITIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
