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    Approved Drug Products containing 75347 listed in the FDA Orange Book. Original Data : FDA Website

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    Actavis Inc

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    01 ACTAVIS LABS FL INC (3)

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    01 CAPSULE, DELAYED REL PELLETS;ORAL (3)

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    01 OMEPRAZOLE (3)

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    OMEPRAZOLE

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    CAPSULE, DELAYED R...
    40MG
    2008-05-30
    75347
    OMEPRAZOLE
    RX
    No
    AB
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    Flag Ireland
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    OMEPRAZOLE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE, DELAYED R...
    10MG
    2008-05-30
    75347
    OMEPRAZOLE
    RX
    No
    AB
    ASK
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    your Marketing & Sales content
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    • FDA
    • EDQM
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    Flag Ireland
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    Digital Content Digital Content

    OMEPRAZOLE

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE, DELAYED R...
    20MG
    2008-05-30
    75347
    OMEPRAZOLE
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
    Upload
    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 75347

    Looking for FDA Orange Book APPLICATION 75347 3

    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 OMEPRAZOLE, with a corresponding application number 75347.

    Regulatory Information RX

    With a dosage strength 40MG

    Dosage Form Route CAPSULE, DELAYED REL PELLETS; ORAL

    Reference Listed Drug No

    Approved since 2008-05-30

    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 OMEPRAZOLE, with a corresponding application number 75347.

    Regulatory Information RX

    With a dosage strength 10MG

    Dosage Form Route CAPSULE, DELAYED REL PELLETS; ORAL

    Reference Listed Drug No

    Approved since 2008-05-30

    Therapeutic Equivalence (TE) Code AB

    17

    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 OMEPRAZOLE, with a corresponding application number 75347.

    Regulatory Information RX

    With a dosage strength 20MG

    Dosage Form Route CAPSULE, DELAYED REL PELLETS; ORAL

    Reference Listed Drug No

    Approved since 2008-05-30

    Therapeutic Equivalence (TE) Code AB

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