"42292-002-20" National Drug Code (NDC)

NDC Code	42292-002-20
Package Description	100 BLISTER PACK in 1 CARTON (42292-002-20) > 1 TABLET in 1 BLISTER PACK (42292-002-01)
Product NDC	42292-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Digitek
Non-Proprietary Name	Digoxin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150506
End Marketing Date	20230228
Marketing Category Name	ANDA
Application Number	ANDA040282
Manufacturer	Mylan Institutional Inc.
Substance Name	DIGOXIN
Strength	.25
Strength Unit	mg/1
Pharmacy Classes	Cardiac Glycoside [EPC], Cardiac Glycosides [CS]