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    FDA Approval for BIJUVA issued to THERAPEUTICSMD INC

    6/24/21 5:13:50 AM ET
    $TXMD
    Biotechnology: Pharmaceutical Preparations
    Health Care
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    New Drug Application (NDA): 210132
    Company: THERAPEUTICSMD INC
    • Email

    Products on NDA 210132

    Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
    BIJUVA ESTRADIOL; PROGESTERONE 1MG;100MG CAPSULE;ORAL Prescription None Yes Yes

    Approval Date(s) and History, Letters, Labels, Reviews for NDA 210132

    Original Approvals or Tentative Approvals
    Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
    10/28/2018 ORIG-1 Approval Type 4 - New Combination STANDARD Label (PDF)
    Letter (PDF)
    Review
    https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210132s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2018/210132Orig1s000Ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/210132Orig1s000TOC.cfm
    Supplements
    Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
    06/22/2021 SUPPL-3 Labeling-Package Insert

    Label is not available on this site.

    06/22/2021 SUPPL-1 Labeling-Package Insert

    Label is not available on this site.

    Labels for NDA 210132

    Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
    Patient Package Insert
    Note Url
    10/28/2018 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210132s000lbl.pdf
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