"42291-081-50" National Drug Code (NDC)

NDC Code	42291-081-50
Package Description	500 TABLET in 1 BOTTLE (42291-081-50)
Product NDC	42291-081
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	20221004
Marketing Category Name	ANDA
Application Number	ANDA208831
Manufacturer	AvKARE
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]