"80005-112-12" National Drug Code (NDC)

NDC Code	80005-112-12
Package Description	120 TABLET in 1 BOTTLE (80005-112-12)
Product NDC	80005-112
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Etravirine
Non-Proprietary Name	Etravirine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20220607
Marketing Category Name	ANDA
Application Number	ANDA215402
Manufacturer	Carnegie Pharmaceuticals LLC
Substance Name	ETRAVIRINE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]