"0378-4890-37" National Drug Code (NDC)

NDC Code	0378-4890-37
Package Description	360 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4890-37)
Product NDC	0378-4890
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20141029
Marketing Category Name	ANDA
Application Number	ANDA205651
Manufacturer	Mylan Pharmaceuticals Inc.
Substance Name	NEVIRAPINE
Strength	400
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]