"49702-202-18" National Drug Code (NDC)

NDC Code	49702-202-18
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (49702-202-18)
Product NDC	49702-202
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	20101019
End Marketing Date	20270228
Marketing Category Name	NDA
Application Number	NDA020857
Manufacturer	ViiV Healthcare Company
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], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA]