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    Digital Content for Prestwick3_000832

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    Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Ribobay has expertise in oligonucleotides from siRNA, Antisense Oligonucleotides, miRNAs, and aptamers & Oligonucleotides CXOs.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Prestwick3_000832

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    $ API Ref.Price (USD/KG) : 441Xls

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    Enforcement Report - Week of February 22, 2023
    Enforcement Report - Week of February 22, 2023

    22 Feb 2023

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-february-22-2023-51785.pdf

    FDA
    22 Feb 2023
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    Hospira Healthcare India Pvt. Ltd. on FDA Import Alert List
    Hospira Healthcare India Pvt. Ltd. on FDA Import Alert List

    01 Aug 2018

    // FDA

    https://www.pharmacompass.com/pdf/news/hospira-healthcare-india-pvt-ltd-on-fda-import-alert-list-1549480434.pdf

    FDA
    01 Aug 2018
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    Cefoxitin for Injection (1 g/vial and 10 g/vial) Recalled by Teva Canada Limited
    Cefoxitin for Injection (1 g/vial and 10 g/vial) Recalled by Teva Canada Limited

    29 Apr 2015

    // Press Release HEALTH CANADA

    http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2015/53139a-eng.php

    Press Release HEALTH CANADA
    29 Apr 2015
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    Walgreens Infusion Services, Ongoing Class II recall of Cefoxitin various strength in normal saline bags because of Lack of sterility assurance.
    Walgreens Infusion Services, Ongoing Class II recall of Cefoxitin various strength in normal saline bags because of Lack of sterility assurance.

    28 Jan 2015

    // FDA

    http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=D-0344-2015&w=01282015&lang=eng

    FDA
    28 Jan 2015
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