"60505-3788-0" National Drug Code (NDC)

NDC Code	60505-3788-0
Package Description	10 BLISTER PACK in 1 CARTON (60505-3788-0) > 10 TABLET in 1 BLISTER PACK
Product NDC	60505-3788
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120522
Marketing Category Name	ANDA
Application Number	ANDA203021
Manufacturer	Apotex Corp
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]