"57237-159-01" National Drug Code (NDC)

NDC Code	57237-159-01
Package Description	100 TABLET in 1 BOTTLE (57237-159-01)
Product NDC	57237-159
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Repaglinide
Non-Proprietary Name	Repaglinide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140122
Marketing Category Name	ANDA
Application Number	ANDA203820
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	REPAGLINIDE
Strength	2
Strength Unit	mg/1
Pharmacy Classes	Glinide [EPC], Potassium Channel Antagonists [MoA]