"0173-0812-59" National Drug Code (NDC)

NDC Code	0173-0812-59
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (0173-0812-59)
Product NDC	0173-0812
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potiga
Non-Proprietary Name	Ezogabine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120419
End Marketing Date	20190731
Marketing Category Name	NDA
Application Number	NDA022345
Manufacturer	GlaxoSmithKline LLC
Substance Name	EZOGABINE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Potassium Channel Openers [MoA],Potassium Channel Opener [EPC]
DEA Schedule	CV