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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022184

Marketing Status: Prescription
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
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