"69452-254-22" National Drug Code (NDC)

NDC Code	69452-254-22
Package Description	120 TABLET in 1 BOTTLE, PLASTIC (69452-254-22)
Product NDC	69452-254
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Etravirine
Non-Proprietary Name	Etravirine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20260101
Marketing Category Name	ANDA
Application Number	ANDA219152
Manufacturer	Bionpharma Inc.
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]