Active Ingredient: BIMATOPROST
Proprietary Name: LUMIGAN
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.01%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N022184
Product Number: 001
Approval Date: Aug 31, 2010
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Prescription
Patent and Exclusivity Information