"51991-331-06" National Drug Code (NDC)

NDC Code	51991-331-06
Package Description	60 TABLET in 1 BOTTLE (51991-331-06)
Product NDC	51991-331
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110411
End Marketing Date	20210531
Marketing Category Name	ANDA
Application Number	ANDA078644
Manufacturer	Breckenridge Pharmaceutical, Inc.
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]