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    Approved Drug Products containing 78470 listed in the FDA Orange Book. Original Data : FDA Website

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    Hikma Pharmaceuticals

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    ACARBOSE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    50MG
    2008-05-07
    78470
    ACARBOSE
    RX
    No
    AB
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    ACARBOSE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    100MG
    2008-05-07
    78470
    ACARBOSE
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
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    your Marketing & Sales content
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    • EDQM
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    ACARBOSE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    25MG
    2008-05-07
    78470
    ACARBOSE
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
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    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 78470

    Looking for FDA Orange Book APPLICATION 78470 3

    19

    Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is ACARBOSE, with a corresponding application number 78470.

    Regulatory Information RX

    With a dosage strength 50MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2008-05-07

    Therapeutic Equivalence (TE) Code AB

    18

    Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is ACARBOSE, with a corresponding application number 78470.

    Regulatory Information RX

    With a dosage strength 100MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2008-05-07

    Therapeutic Equivalence (TE) Code AB

    17

    Hikma Pharmaceuticals, based in United Kingdom, is a pharmaceutical company that stands out with its certifications from FDA and EDQM.

    One of their notable products is ACARBOSE, with a corresponding application number 78470.

    Regulatory Information RX

    With a dosage strength 25MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug No

    Approved since 2008-05-07

    Therapeutic Equivalence (TE) Code AB

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