"45963-568-32" National Drug Code (NDC)

NDC Code	45963-568-32
Package Description	500 TABLET in 1 BOTTLE (45963-568-32)
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
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]