"0597-0046-41" National Drug Code (NDC)

NDC Code	0597-0046-41
Package Description	1 BLISTER PACK in 1 CARTON (0597-0046-41) > 14 TABLET in 1 BLISTER PACK
Product NDC	0597-0046
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Viramune
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20010801
Marketing Category Name	NDA
Application Number	NDA020636
Manufacturer	Boehringer Ingelheim Pharmaceuticals Inc.
Substance Name	NEVIRAPINE
Strength	200
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]