"0597-0123-03" National Drug Code (NDC)

NDC Code	0597-0123-03
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0597-0123-03)
Product NDC	0597-0123
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Viramune
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20110411
Marketing Category Name	NDA
Application Number	NDA201152
Manufacturer	Boehringer Ingelheim 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]