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    Benzonatate

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    Enforcement Report - Week of January 31, 2024
    Enforcement Report - Week of January 31, 2024

    31 Jan 2024

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-january-31-2024-59527.pdf

    FDA
    31 Jan 2024
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    FDA warns of rise in reports of child poisonings linked to cough medicine
    FDA warns of rise in reports of child poisonings linked to cough medicine

    15 Nov 2022

    // NBC NEWS

    https://www.nbcnews.com/health/health-news/fda-warns-rise-reports-child-poisonings-linked-cough-medicine-rcna57065

    NBC NEWS
    15 Nov 2022
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    Puracap Pharm's Generic Benzonatate Receives Approval in US
    Puracap Pharm's Generic Benzonatate Receives Approval in US

    19 Dec 2018

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=206948

    FDA
    19 Dec 2018
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    Aiping Pharm's Generic Benzonatate Receives Approval in US
    Aiping Pharm's Generic Benzonatate Receives Approval in US

    13 Nov 2018

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=210562

    FDA
    13 Nov 2018
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    Enforcement Report - Week of May 31, 2017
    Enforcement Report - Week of May 31, 2017

    31 May 2017

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-may-31-2017-1496224025.pdf

    FDA
    31 May 2017
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    American Health Packaging, Ongoing Class II recall of Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose) because of Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
    American Health Packaging, Ongoing Class II recall of Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose) because of Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules

    08 Apr 2015

    // FDA

    http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=D-0430-2015&w=04082015&lang=eng

    FDA
    08 Apr 2015
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