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    List of All Manufacturers & Suppliers for 21001 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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    Johnson & Johnson Innovative Medicine

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    01 ALMOTRIPTAN MALATE (2)

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    01 JANSSEN PHARMS (2)

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    01 TABLET;ORAL (2)

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    01 EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

    02 EQ 6.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

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    Almotriptan Malate

    PDF Supplier PDF
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    TABLET;ORAL
    EQ 6.25MG BASE **Feder...
    AXERT
    USA
    21001
    2001-05-07
    DISCN
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    your Marketing & Sales content
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    • FDA
    • EDQM
    Virtual Booth Upload your Marketing & Sales content on your company Virtual Booth, click HERE
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    Almotriptan Malate

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET;ORAL
    EQ 12.5MG BASE **Feder...
    AXERT
    USA
    21001
    2001-05-07
    DISCN
    ASK
    US
    PHARMACOMPASS
    Upload
    your Marketing & Sales content

    Looking for CTD TGA MCC DOSSIER APPLICATION 21001

    Looking for CTD TGA MCC DOSSIER APPLICATION 21001 2

    19

    Johnson & Johnson Innovative Medicine, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is ALMOTRIPTAN MALATE, with a corresponding application number 21001 and regulatory information .

    proudly manufactured in the

    approval since 2001-05-07

    Johnson & Johnson Innovative Medicine's AXERT TABLET;ORAL, medication with EQ 6.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** of ALMOTRIPTAN MALATE.

    18

    Johnson & Johnson Innovative Medicine, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is ALMOTRIPTAN MALATE, with a corresponding application number 21001 and regulatory information .

    proudly manufactured in the

    approval since 2001-05-07

    Johnson & Johnson Innovative Medicine's AXERT TABLET;ORAL, medication with EQ 12.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** of ALMOTRIPTAN MALATE.

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