"49702-217-18" National Drug Code (NDC)

Trizivir 60 TABLET, FILM COATED in 1 BOTTLE (49702-217-18)
(ViiV Healthcare Company)

NDC Code49702-217-18
Package Description60 TABLET, FILM COATED in 1 BOTTLE (49702-217-18)
Product NDC49702-217
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTrizivir
Non-Proprietary NameAbacavir Sulfate, Lamivudine, And Zidovudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101102
End Marketing Date20241130
Marketing Category NameNDA
Application NumberNDA021205
ManufacturerViiV Healthcare Company
Substance NameABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE
Strength300; 150; 300
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesCytochrome P450 1A1 Inhibitors [MoA], 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], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA]

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