"71335-0141-3" National Drug Code (NDC)

NDC Code	71335-0141-3
Package Description	4 TABLET in 1 BOTTLE (71335-0141-3)
Product NDC	71335-0141
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lamivudine And Zidovudine
Non-Proprietary Name	Lamivudine And Zidovudine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20161210
Marketing Category Name	ANDA
Application Number	ANDA079128
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]