"31722-505-10" National Drug Code (NDC)

NDC Code	31722-505-10
Package Description	1000 TABLET in 1 BOTTLE (31722-505-10)
Product NDC	31722-505
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120523
Marketing Category Name	ANDA
Application Number	ANDA078584
Manufacturer	Camber Pharmaceuticals, Inc.
Substance Name	NEVIRAPINE
Strength	200
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]