"67877-510-37" National Drug Code (NDC)

NDC Code	67877-510-37
Package Description	5 BLISTER PACK in 1 CARTON (67877-510-37) / 10 TABLET in 1 BLISTER PACK (67877-510-33)
Product NDC	67877-510
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	20171224
Marketing Category Name	ANDA
Application Number	ANDA209222
Manufacturer	Ascend Laboratories, LLC
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]