"61919-669-02" National Drug Code (NDC)

Truvada 2 TABLET, FILM COATED in 1 BOTTLE (61919-669-02)
(DIRECT RX)

NDC Code61919-669-02
Package Description2 TABLET, FILM COATED in 1 BOTTLE (61919-669-02)
Product NDC61919-669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTruvada
Non-Proprietary NameEmtricitabine And Tenofovir Disoproxil Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170222
Marketing Category NameNDA
Application NumberNDA021752
ManufacturerDIRECT RX
Substance NameEMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Strength200; 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], Nucleosides [CS], Nucleosides [CS]

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