"0169-0082-82" National Drug Code (NDC)

NDC Code	0169-0082-82
Package Description	500 TABLET in 1 BOTTLE, PLASTIC (0169-0082-82)
Product NDC	0169-0082
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Prandin
Non-Proprietary Name	Repaglinide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20000103
End Marketing Date	20201031
Marketing Category Name	NDA
Application Number	NDA020741
Manufacturer	Novo Nordisk
Substance Name	REPAGLINIDE
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Glinide [EPC],Potassium Channel Antagonists [MoA]