"0781-5893-31" National Drug Code (NDC)

NDC Code	0781-5893-31
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5893-31)
Product NDC	0781-5893
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20140415
Marketing Category Name	ANDA
Application Number	ANDA203411
Manufacturer	Sandoz Inc
Substance Name	NEVIRAPINE
Strength	400
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]