"42571-131-29" National Drug Code (NDC)

NDC Code	42571-131-29
Package Description	6 BLISTER PACK in 1 CARTON (42571-131-29) > 10 TABLET in 1 BLISTER PACK
Product NDC	42571-131
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	ANDA203080
Manufacturer	Micro Labs Limited
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]