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    Approved Drug Products containing 90797 listed in the FDA Orange Book. Original Data : FDA Website

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    Actavis Inc

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    01 ACTAVIS TOTOWA (2)

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    01 TABLET, DELAYED RELEASE;ORAL (2)

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    01 PANTOPRAZOLE SODIUM (2)

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    PANTOPRAZOLE SODIUM

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    TABLET, DELAYED RE...
    EQ 40MG BASE
    2011-02-07
    90797
    PANTOPRAZOLE SODIU...
    RX
    No
    AB
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    Flag Ireland
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    PANTOPRAZOLE SODIUM

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET, DELAYED RE...
    EQ 20MG BASE
    2011-02-07
    90797
    PANTOPRAZOLE SODIU...
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
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    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 90797

    Looking for FDA Orange Book APPLICATION 90797 2

    19

    Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is PANTOPRAZOLE SODIUM, with a corresponding application number 90797.

    Regulatory Information RX

    With a dosage strength EQ 40MG BASE

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2011-02-07

    Therapeutic Equivalence (TE) Code AB

    18

    Actavis Inc, based in Ireland, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is PANTOPRAZOLE SODIUM, with a corresponding application number 90797.

    Regulatory Information RX

    With a dosage strength EQ 20MG BASE

    Dosage Form Route TABLET, DELAYED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2011-02-07

    Therapeutic Equivalence (TE) Code AB

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