"0115-1387-08" National Drug Code (NDC)

NDC Code	0115-1387-08
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (0115-1387-08)
Product NDC	0115-1387
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ezetimibe And Simvastatin
Non-Proprietary Name	Ezetimibe And Simvastatin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20170426
End Marketing Date	20200331
Marketing Category Name	ANDA
Application Number	ANDA201890
Manufacturer	Impax Generics
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]