POTIGA

Product NDC

0173-0812

11-digit product format

001730812

Labeler code

0173

Product ID

0173-0812_38028c77-169f-47e4-9d61-5f625f3627f3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ezogabine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

GlaxoSmithKline LLC

Application

NDA022345

Marketing category

NDA

Marketing start

2012-04-19

Marketing end

2019-07-31

Substance

EZOGABINE

Active strength

200 mg/1

Pharmacologic classes

Potassium Channel Openers [MoA],Potassium Channel Opener [EPC]

DEA schedule

CV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record