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    List of All Manufacturers & Suppliers for 9388 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    Teva Pharmaceutical Industries

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    01 ACETAZOLAMIDE SODIUM (1)

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    01 TEVA WOMENS (1)

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    01 INJECTABLE;INJECTION (1)

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    01 EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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    01 USA (1)

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    Acetazolamide Sodium

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    INJECTABLE;INJECTION
    EQ 500MG BASE/VIAL **F...
    DIAMOX
    USA
    9388
    1982-01-01
    DISCN
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    Looking for CTD TGA MCC DOSSIER APPLICATION 9388

    Looking for CTD TGA MCC DOSSIER APPLICATION 9388 1

    19

    Teva Pharmaceutical Industries, based in Israel, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is ACETAZOLAMIDE SODIUM, with a corresponding application number 9388 and regulatory information .

    proudly manufactured in the

    approval since 1982-01-01

    Teva Pharmaceutical Industries's DIAMOX INJECTABLE;INJECTION, medication with EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** of ACETAZOLAMIDE SODIUM.

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