"49349-683-04" National Drug Code (NDC)

NDC Code	49349-683-04
Package Description	14 TABLET, FILM COATED in 1 BLISTER PACK (49349-683-04)
Product NDC	49349-683
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	20130423
Marketing Category Name	NDA
Application Number	NDA020857
Manufacturer	REMEDYREPACK INC.
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]