"0054-0459-21" National Drug Code (NDC)

NDC Code	0054-0459-21
Package Description	60 TABLET in 1 BOTTLE (0054-0459-21)
Product NDC	0054-0459
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120521
End Marketing Date	20200711
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA020636
Manufacturer	West-Ward Pharmaceuticals Corp.
Substance Name	NEVIRAPINE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA]