"0378-4050-80" National Drug Code (NDC)

NDC Code	0378-4050-80
Package Description	180 TABLET in 1 BOTTLE, PLASTIC (0378-4050-80)
Product NDC	0378-4050
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120522
Marketing Category Name	ANDA
Application Number	ANDA202523
Manufacturer	Mylan Pharmaceuticals 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 [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA]