NDC 15584-0101

Atripla

Efavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate

Atripla is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Gilead Sciences, Llc. The primary component is Efavirenz; Emtricitabine; Tenofovir Disoproxil Fumarate.

Product ID15584-0101_3cf1ef4b-a2c0-416a-80be-59c4d65d2dfc
NDC15584-0101
Product TypeHuman Prescription Drug
Proprietary NameAtripla
Generic NameEfavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2006-07-20
Marketing CategoryNDA / NDA
Application NumberNDA021937
Labeler NameGilead Sciences, LLC
Substance NameEFAVIRENZ; EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
Active Ingredient Strength600 mg/1; mg/1; mg/1
Pharm ClassesHuman Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],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],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 15584-0101-1

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (15584-0101-1)
Marketing Start Date2006-07-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15584-0101-1 [15584010101]

Atripla TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021937
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-07-20

Drug Details

Active Ingredients

IngredientStrength
EFAVIRENZ600 mg/1

OpenFDA Data

SPL SET ID:2e97aa6d-09f7-46df-9499-63db7e9bac35
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 643070
  • 643066
  • Pharmacological Class

    • Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]
    • Non-Nucleoside Analog [EXT]
    • 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]
    • Nucleoside Analog [EXT]
    • 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 [EXT]
    • Nucleoside Reverse Transcriptase Inhibitors [MoA]
    • Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]

    Medicade Reported Pricing

    15584010101 ATRIPLA TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Atripla" or generic name "Efavirenz, Emtricitabine, And Tenofovir Disoproxil Fumarate"

    NDCBrand NameGeneric Name
    15584-0101Atriplaefavirenz, emtricitabine, and tenofovir disoproxil fumarate
    50090-0980Atriplaefavirenz, emtricitabine, and tenofovir disoproxil fumarate
    53808-0208Atriplaefavirenz, emtricitabine, and tenofovir disoproxil fumarate
    70518-0341Atriplaefavirenz, emtricitabine, and tenofovir disoproxil fumarate

    Trademark Results [Atripla]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ATRIPLA
    ATRIPLA
    78595551 3276743 Live/Registered
    GILEAD SCIENCES LLC
    2005-03-25

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