"0173-0595-02" National Drug Code (NDC)

NDC Code	0173-0595-02
Package Description	120 TABLET, FILM COATED in 1 DOSE PACK (0173-0595-02)
Product NDC	0173-0595
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Combivir
Non-Proprietary Name	Lamivudine And Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19970930
End Marketing Date	20140731
Marketing Category Name	NDA
Application Number	NDA020857
Manufacturer	GlaxoSmithKline LLC
Substance Name	LAMIVUDINE; ZIDOVUDINE
Strength	150; 300
Strength Unit	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 [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]