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    List of All Manufacturers & Suppliers for 22106 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    Shionogi

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    01 DORIPENEM (2)

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    01 SHIONOGI INC (2)

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    01 INJECTABLE;INTRAVENOUS (2)

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    01 250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

    02 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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    01 USA (2)

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      Doripenem

      PDF Supplier PDF
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      INJECTABLE;INTRAVENOUS
      500MG/VIAL **Federal R...
      DORIBAX
      USA
      22106
      2007-10-12
      DISCN
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      US
      PHARMACOMPASS
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      your Marketing & Sales content
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        Flag Japan
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        Doripenem

        PDF Supplier PDF
        URL Supplier Web Content
        INJECTABLE;INTRAVENOUS
        250MG/VIAL **Federal R...
        DORIBAX
        USA
        22106
        2010-10-05
        DISCN
        ASK
        US
        PHARMACOMPASS
        Upload
        your Marketing & Sales content

        Looking for CTD TGA MCC DOSSIER APPLICATION 22106

        Looking for CTD TGA MCC DOSSIER APPLICATION 22106 2

        19

        Shionogi, based in Japan, is a pharmaceutical company.

        One of their notable products is DORIPENEM, with a corresponding application number 22106 and regulatory information .

        proudly manufactured in the

        approval since 2007-10-12

        Shionogi's DORIBAX INJECTABLE;INTRAVENOUS, medication with 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** of DORIPENEM.

        18

        Shionogi, based in Japan, is a pharmaceutical company.

        One of their notable products is DORIPENEM, with a corresponding application number 22106 and regulatory information .

        proudly manufactured in the

        approval since 2010-10-05

        Shionogi's DORIBAX INJECTABLE;INTRAVENOUS, medication with 250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** of DORIPENEM.

        Post Enquiry
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