"45963-568-08" National Drug Code (NDC)

NDC Code	45963-568-08
Package Description	90 TABLET in 1 BOTTLE (45963-568-08)
Product NDC	45963-568
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ezetimibe And Simvastatin
Non-Proprietary Name	Ezetimibe And Simvastatin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170426
End Marketing Date	20260228
Marketing Category Name	ANDA
Application Number	ANDA202968
Manufacturer	Actavis Pharma, Inc.
Substance Name	EZETIMIBE; SIMVASTATIN
Strength	10; 80
Strength Unit	mg/1; mg/1
Pharmacy Classes	Decreased Cholesterol Absorption [PE], Dietary Cholesterol Absorption Inhibitor [EPC], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]