"63629-4872-3" National Drug Code (NDC)

NDC Code	63629-4872-3
Package Description	4 TABLET, FILM COATED in 1 BOTTLE (63629-4872-3)
Product NDC	63629-4872
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine And Zidovudine
Non-Proprietary Name	Lamivudine And Zidovudine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120515
End Marketing Date	20221231
Marketing Category Name	ANDA
Application Number	ANDA202418
Manufacturer	Bryant Ranch Prepack
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]