"54569-5805-0" National Drug Code (NDC)

Atripla 30 TABLET, FILM COATED in 1 BOTTLE (54569-5805-0)
(A-S Medication Solutions)

NDC Code54569-5805-0
Package Description30 TABLET, FILM COATED in 1 BOTTLE (54569-5805-0)
Product NDC54569-5805
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtripla
Non-Proprietary NameEfavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060720
Marketing Category NameNDA
Application NumberNDA021937
ManufacturerA-S Medication Solutions
Substance NameEFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength600; 200; 300
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesHuman Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C9 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],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],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

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