"71335-1916-2" National Drug Code (NDC)

Lamivudine And Zidovudine 60 TABLET in 1 BOTTLE (71335-1916-2)
(Bryant Ranch Prepack)

NDC Code71335-1916-2
Package Description60 TABLET in 1 BOTTLE (71335-1916-2)
Product NDC71335-1916
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamivudine And Zidovudine
Non-Proprietary NameLamivudine And Zidovudine
Dosage FormTABLET
UsageORAL
Start Marketing Date20180830
Marketing Category NameANDA
Application NumberANDA090679
ManufacturerBryant Ranch Prepack
Substance NameLAMIVUDINE; ZIDOVUDINE
Strength150; 300
Strength Unitmg/1; mg/1
Pharmacy ClassesHepatitis 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]

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