Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 022184

LUMIGAN (BIMATOPROST)
0.01% 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: ALLERGAN INC
Marketing Status:  Prescription
Patent and Exclusivity Information

Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English