"16714-780-01" National Drug Code (NDC)

NDC Code	16714-780-01
Package Description	30 TABLET in 1 BOTTLE (16714-780-01)
Product NDC	16714-780
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	20190819
End Marketing Date	20261031
Marketing Category Name	ANDA
Application Number	ANDA208699
Manufacturer	NORTHSTAR RX LLC
Substance Name	EZETIMIBE; SIMVASTATIN
Strength	10; 40
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]