"0378-6950-05" National Drug Code (NDC)

NDC Code	0378-6950-05
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6950-05)
Product NDC	0378-6950
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20151109
Marketing Category Name	ANDA
Application Number	ANDA206271
Manufacturer	Mylan Pharmaceuticals Inc.
Substance Name	NEVIRAPINE
Strength	100
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]