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    • Naloxone hydrochloride

    Metadata Updated: February 18, 2026

    Naloxone Hydrochloride is an injectable prescription medication that reverses opioid overdoses by blocking opioid effects in the body. Available in strengths of 0.4 mg/mL and 1 mg/mL, it is administered via intramuscular, intravenous, or subcutaneous injection. Manufactured by Hikma Pharmaceuticals USA Inc. under ANDA212300. 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 ANDA213209
    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 df1a458f-f810-42f1-aa5a-42527bda97d8
    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 3f04fb0cb86ba1f3340208e892832cf18decb0627079914cfc08d551d7e975c8
    Source Schema Version 1.1

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