"70518-0341-0" National Drug Code (NDC)

Atripla 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0341-0)
(REMEDYREPACK INC.)

NDC Code70518-0341-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0341-0)
Product NDC70518-0341
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtripla
Non-Proprietary NameEfavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170320
Marketing Category NameNDA
Application NumberNDA021937
ManufacturerREMEDYREPACK INC.
Substance NameEFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength600; 200; 300
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesCytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleoside Reverse Transcriptase Inhibitors [MoA], Nucleosides [CS], Nucleosides [CS]

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