"55289-002-30" National Drug Code (NDC)

NDC Code	55289-002-30
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (55289-002-30)
Product NDC	55289-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Digoxin
Non-Proprietary Name	Digoxin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20020726
Marketing Category Name	ANDA
Application Number	ANDA076268
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	DIGOXIN
Strength	125
Strength Unit	ug/1
Pharmacy Classes	Cardiac Glycoside [EPC],Cardiac Glycosides [CS]