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    FDA Approval for BIKTARVY issued to GILEAD SCIENCES INC

    10/22/24 4:04:28 PM ET
    $GILD
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care
    Get the next $GILD alert in real time by email
    New Drug Application (NDA): 210251
    Company: GILEAD SCIENCES INC
    • Email

    Products on NDA 210251

    Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
    BIKTARVY BICTEGRAVIR SODIUM; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE EQ 50MG BASE;200MG;EQ 25MG BASE TABLET;ORAL Prescription None Yes Yes
    BIKTARVY BICTEGRAVIR SODIUM; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE EQ 30MG BASE;120MG;EQ 15MG BASE TABLET;ORAL Prescription None Yes No

    Approval Date(s) and History, Letters, Labels, Reviews for NDA 210251

    Original Approvals or Tentative Approvals
    Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
    02/07/2018 ORIG-1 Approval Type 1 - New Molecular Entity and Type 4 - New Combination PRIORITY; Orphan Label (PDF)
    Letter (PDF)
    Review
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210251s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/210251Orig1s000Ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/210251Orig1s000TOC.cfm
    Supplements
    Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
    10/08/2024 SUPPL-20 Label (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251Orig1s020lbl.pdf
    04/24/2024 SUPPL-19 Efficacy-Labeling Change With Clinical Data Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251s019lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/210251Orig1s019ltr.pdf
    02/23/2024 SUPPL-18 Efficacy-New Indication Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251s018lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/210251Orig1s018ltr.pdf
    05/01/2023 SUPPL-17 Labeling-Container/Carton Labels Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/210251Orig1s017lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/210251Orig1s017ltr.pdf
    10/14/2022 SUPPL-15 Efficacy-Labeling Change With Clinical Data Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/210251s015lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/210251Orig1s015ltr.pdf
    10/07/2021 SUPPL-14 Efficacy-New Patient Population Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s014lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s014ltr.pdf
    09/10/2021 SUPPL-13 Labeling-Patient Package Insert, Labeling-Package Insert Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s013lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s013ltr.pdf
    03/04/2021 SUPPL-10 Labeling-Package Insert Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s010lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s010ltr.pdf
    02/11/2021 SUPPL-9 Labeling-Package Insert, Labeling-Patient Package Insert Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s009lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s009ltr.pdf
    02/24/2021 SUPPL-8 Efficacy-Labeling Change With Clinical Data Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s008lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s008ltr.pdf
    02/05/2021 SUPPL-7 Efficacy-New Patient Population Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s007lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/210251Orig1s007ltr.pdf
    08/02/2019 SUPPL-6 Labeling-Package Insert Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/210251s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/210251Orig1s006ltr.pdf
    06/18/2019 SUPPL-5 Efficacy-New Patient Population Label (PDF)
    Letter (PDF)
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/210251s005lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/210251Orig1s005ltr.pdf

    Labels for NDA 210251

    Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
    Patient Package Insert
    Note Url
    10/08/2024 SUPPL-20 Manufacturing (CMC) Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251Orig1s020lbl.pdf
    04/24/2024 SUPPL-19 Efficacy-Labeling Change With Clinical Data Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251s019lbl.pdf
    02/23/2024 SUPPL-18 Efficacy-New Indication Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/210251s018lbl.pdf
    05/01/2023 SUPPL-17 Labeling-Container/Carton Labels Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/210251Orig1s017lbl.pdf
    10/14/2022 SUPPL-15 Efficacy-Labeling Change With Clinical Data Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/210251s015lbl.pdf
    10/07/2021 SUPPL-14 Efficacy-New Patient Population Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s014lbl.pdf
    09/10/2021 SUPPL-13 Labeling-Patient Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s013lbl.pdf
    09/10/2021 SUPPL-13 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s013lbl.pdf
    03/04/2021 SUPPL-10 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s010lbl.pdf
    02/24/2021 SUPPL-8 Efficacy-Labeling Change With Clinical Data Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s008lbl.pdf
    02/11/2021 SUPPL-9 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s009lbl.pdf
    02/11/2021 SUPPL-9 Labeling-Patient Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s009lbl.pdf
    02/05/2021 SUPPL-7 Efficacy-New Patient Population Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210251s007lbl.pdf
    08/02/2019 SUPPL-6 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/210251s006lbl.pdf
    06/18/2019 SUPPL-5 Efficacy-New Patient Population Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/210251s005lbl.pdf
    02/07/2018 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210251s000lbl.pdf
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