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    • Lasmiditan

    Metadata Updated: February 18, 2026

    Reyvow (lasmiditan) is a prescription oral tablet medication manufactured by Eli Lilly and Company, available in 50 mg and 100 mg strengths to treat acute migraines. The 200 mg strength has been discontinued. It is a controlled substance (CV schedule). This information was generated using AI and is provided for informational and research purposes only.

    Access & Use Information

    Public: This dataset is intended for public access and use. License: See this page for license information.

    Downloads & Resources

    Dates

    Metadata Created Date February 18, 2026
    Metadata Updated Date February 18, 2026
    Data Update Frequency R/P1Y

    Metadata Source

    Harvested from Healthdata.gov

    Other Data Resources

    Additional Metadata

    Resource Type Dataset
    Metadata Created Date February 18, 2026
    Metadata Updated Date February 18, 2026
    Publisher U.S. Food and Drug Administration
    Maintainer
    Identifier ANDA211280
    Data First Published 2016-09-16
    Data Last Modified 2025-03-17
    Category FDA
    Public Access Level public
    Data Update Frequency R/P1Y
    Bureau Code 009:10
    Metadata Context https://project-open-data.cio.gov/v1.1/schema/catalog.jsonld
    Metadata Catalog ID https://healthdata.gov/data.json
    Schema Version https://project-open-data.cio.gov/v1.1/schema
    Catalog Describedby https://project-open-data.cio.gov/v1.1/schema/catalog.json
    Harvest Object Id 191ebe5a-6cee-4468-804c-fa3664568b32
    Harvest Source Id 651e43b2-321c-4e4c-b86a-835cfc342cb0
    Harvest Source Title Healthdata.gov
    Homepage URL https://www.fda.gov/drugs
    License https://open.fda.gov/license
    Program Code 009:002
    Source Datajson Identifier True
    Source Hash 70b32df1501c35a4f9a1ffc76385ce877766ce2788def8a7eb8568eb14e44120
    Source Schema Version 1.1

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