"33342-238-12" National Drug Code (NDC)

NDC Code	33342-238-12
Package Description	10 BLISTER PACK in 1 CARTON (33342-238-12) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	33342-238
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20171007
Marketing Category Name	ANDA
Application Number	ANDA206879
Manufacturer	Macleods Pharmaceuticals Limited
Substance Name	NEVIRAPINE
Strength	400
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]