"0173-0249-80" National Drug Code (NDC)

NDC Code	0173-0249-80
Package Description	5000 TABLET in 1 BOTTLE (0173-0249-80)
Product NDC	0173-0249
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lanoxin
Non-Proprietary Name	Digoxin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19840702
End Marketing Date	20150930
Marketing Category Name	NDA
Application Number	NDA020405
Manufacturer	GlaxoSmithKline LLC
Substance Name	DIGOXIN
Strength	250
Strength Unit	ug/1
Pharmacy Classes	Cardiac Glycoside [EPC],Cardiac Glycosides [Chemical/Ingredient]