LUMIGAN - 0023-3205-03 - (bimatoprost)

Alphabetical Index


Drug Information of LUMIGAN

Product NDC: 0023-3205
Proprietary Name: LUMIGAN
Non Proprietary Name: bimatoprost
Active Ingredient(s): .1    mg/mL & nbsp;   bimatoprost
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of LUMIGAN

Product NDC: 0023-3205
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022184
Marketing Category: NDA
Start Marketing Date: 20100910

Package Information of LUMIGAN

Package NDC: 0023-3205-03
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0023-3205-03) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of LUMIGAN

NDC Code 0023-3205-03
Proprietary Name LUMIGAN
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0023-3205-03) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 0023-3205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bimatoprost
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20100910
Marketing Category Name NDA
Labeler Name Allergan, Inc.
Substance Name BIMATOPROST
Strength Number .1
Strength Unit mg/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of LUMIGAN


General Information