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    Aurobindo Pharma Issues Voluntary Nationwide Recall for Acetaminophen, Aspirin
    Aurobindo Pharma Issues Voluntary Nationwide Recall for Acetaminophen, Aspirin

    24 Jul 2024

    // FDA

    https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aurobindo-pharma-usa-inc-behalf-aurohealth-issues-voluntary-nationwide-recall-one-1-lot-healthy

    FDA
    24 Jul 2024
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    Quagen's Generic Butalbital, Acetaminophen and Caffeine Receives Approval in the U.S.
    Quagen's Generic Butalbital, Acetaminophen and Caffeine Receives Approval in the U.S.

    12 Mar 2024

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=216376

    FDA
    12 Mar 2024
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    Hikma's Generic Dabigatran Etexilate Mesylate Receives Approval in the U.S.
    Hikma's Generic Dabigatran Etexilate Mesylate Receives Approval in the U.S.

    25 Mar 2022

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215135

    FDA
    25 Mar 2022
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    Seton & Senores Pharma, launch Butalbital, Acetaminophen, Caffeine Capsules
    Seton & Senores Pharma, launch Butalbital, Acetaminophen, Caffeine Capsules

    17 Mar 2022

    // PRNEWSWIRE

    https://www.prnewswire.com/news-releases/seton-pharmaceuticals-llc-and-senores-pharmaceuticals-inc-launch-butalbital-acetaminophen-and-caffeine-capsules-usp-50-mg325-mg40-mg-in-the-us-market-301505001.html

    PRNEWSWIRE
    17 Mar 2022
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    Aurobindo's Generic Acetaminophen, Aspirin & Caffeine Receives Approval in U.S.
    Aurobindo's Generic Acetaminophen, Aspirin & Caffeine Receives Approval in U.S.

    02 Feb 2022

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211695

    FDA
    02 Feb 2022
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    Hikma's Generic Butalbital, Acetaminophen, Caffeine Receives Approval in U.S.
    Hikma's Generic Butalbital, Acetaminophen, Caffeine Receives Approval in U.S.

    26 Jan 2022

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215138

    FDA
    26 Jan 2022
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