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    Home > Medical News > Latest Medical News > Announcement of the State Food and Drug Administration on the conversion of glucosamine sulfate effervescent tablets and glucosamine sulfate granules prescription drugs to over-the-counter drugs (No. 1 in 2020

    Announcement of the State Food and Drug Administration on the conversion of glucosamine sulfate effervescent tablets and glucosamine sulfate granules prescription drugs to over-the-counter drugs (No. 1 in 2020

    • Last Update: 2021-07-07
    • Source: Internet
    • Author: User
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    According to the "Administrative Measures for the Classification of Prescription Drugs and Over-the-Counter Drugs (for Trial Implementation)" (State Drug Administration Order No.
    10), after the State Drug Administration’s organization of demonstration and review, glucosamine sulfate effervescent tablets and glucosamine sulfate granules are two Medicines are converted from prescription drugs to over-the-counter drugs
    .


    The list of varieties and the template of non-prescription drug instructions will be released together


    The holders of the relevant drug marketing authorizations are requested to submit to the provincial drug regulatory authority for the record of the revised inserts in accordance with the "Administrative Measures for Drug Registration" and other relevant regulations before August 31, 2021, and promptly notify the relevant medical institutions and medical institutions of the revised contents of the inserts.
    Units such as pharmaceutical business enterprises
    .

    The contents of the non-prescription drug inserts other than those specified in the template inserts shall be implemented in accordance with the original approval documents
    .


    If the drug label involves related content, it should be revised together


    Hereby announce
    .


    Attachment: 1.


    List of varieties

    2.
    Templates for non-prescription drug instructions




    State Food and Drug Administration

    December 1, 2020

    Announcement No.


    133 of 2020 Annex 1.
    doc of the National Medical Products Administration

    Announcement No.


    133 of 2020, Annex 2 of the National Medical Products Administration.




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