"42571-166-60" National Drug Code (NDC)

NDC Code	42571-166-60
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (42571-166-60)
Product NDC	42571-166
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine, Nevirapine, And Zidovudine
Non-Proprietary Name	Lamivudine, Nevirapine, And Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20180903
Marketing Category Name	NDA
Application Number	NDA205626
Manufacturer	Micro Labs Limited
Substance Name	LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE
Strength	150; 200; 300
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]