"51079-456-20" National Drug Code (NDC)

NDC Code	51079-456-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-456-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-456-01)
Product NDC	51079-456
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Simvastatin
Non-Proprietary Name	Simvastatin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20060710
End Marketing Date	20200531
Marketing Category Name	ANDA
Application Number	ANDA076052
Manufacturer	Mylan Institutional Inc.
Substance Name	SIMVASTATIN
Strength	40
Strength Unit	mg/1
Pharmacy Classes	HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]