"24236-292-22" National Drug Code (NDC)

Atripla 150 TABLET, FILM COATED in 1 CANISTER (24236-292-22)
(REMEDYREPACK INC.)

NDC Code24236-292-22
Package Description150 TABLET, FILM COATED in 1 CANISTER (24236-292-22)
Product NDC24236-292
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAtripla
Non-Proprietary NameEfavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130329
Marketing Category NameNDA
Application NumberNDA021937
ManufacturerREMEDYREPACK INC.
Substance NameEFAVIRENZ
Strength600
Strength Unitmg/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]

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