"47781-342-01" National Drug Code (NDC)

NDC Code	47781-342-01
Package Description	100 TABLET in 1 BOTTLE (47781-342-01)
Product NDC	47781-342
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acarbose
Non-Proprietary Name	Acarbose
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20080130
End Marketing Date	20211231
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA020482
Manufacturer	Alvogen, Inc.
Substance Name	ACARBOSE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]