"53150-209-06" National Drug Code (NDC)

NDC Code	53150-209-06
Package Description	60 TABLET in 1 BOTTLE (53150-209-06)
Product NDC	53150-209
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140430
Marketing Category Name	ANDA
Application Number	ANDA078195
Manufacturer	Amneal-Agila, LLC
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 [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA]