POTIGA - 0173-0813-59 - (ezogabine)

Alphabetical Index


Drug Information of POTIGA

Product NDC: 0173-0813
Proprietary Name: POTIGA
Non Proprietary Name: ezogabine
Active Ingredient(s): 300    mg/1 & nbsp;   ezogabine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of POTIGA

Product NDC: 0173-0813
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022345
Marketing Category: NDA
Start Marketing Date: 20120419

Package Information of POTIGA

Package NDC: 0173-0813-59
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (0173-0813-59)

NDC Information of POTIGA

NDC Code 0173-0813-59
Proprietary Name POTIGA
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (0173-0813-59)
Product NDC 0173-0813
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ezogabine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120419
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name EZOGABINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Potassium Channel Openers [MoA],Potassium Channel Opener [EPC]

Complete Information of POTIGA


General Information