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    Approved Drug Products containing 18422 listed in the FDA Orange Book. Original Data : FDA Website

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    Pfizer Inc

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    01 PFIZER PHARMS (3)

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    01 CAPSULE;ORAL (2)

    02 TABLET;ORAL (1)

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    01 DISCN (2)

    02 RX (1)

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    01 LOPID (3)

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    01 No (2)

    02 Yes (1)

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    GEMFIBROZIL

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE; ORAL
    300MG
    1982-01-01
    18422
    LOPID
    DISCN
    No
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    GEMFIBROZIL

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET; ORAL
    600MG
    1986-11-20
    18422
    LOPID
    RX
    Yes
    AB
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    GEMFIBROZIL

    PDF Supplier PDF
    URL Supplier Web Content
    CAPSULE; ORAL
    200MG
    1982-01-01
    18422
    LOPID
    DISCN
    No
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    your Marketing & Sales content

    Looking for FDA Orange Book APPLICATION 18422

    Looking for FDA Orange Book APPLICATION 18422 3

    19

    Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is GEMFIBROZIL, with a corresponding application number 18422.

    Regulatory Information DISCN

    With a dosage strength 300MG

    Dosage Form Route CAPSULE; ORAL

    Reference Listed Drug No

    Approved since 1982-01-01

    18

    Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is GEMFIBROZIL, with a corresponding application number 18422.

    Regulatory Information RX

    With a dosage strength 600MG

    Dosage Form Route TABLET; ORAL

    Reference Listed Drug Yes

    Approved since 1986-11-20

    Therapeutic Equivalence (TE) Code AB

    17

    Pfizer Inc, based in U.S.A, is a pharmaceutical company that stands out with its certifications from FDA, EDQM and WHO-GMP.

    One of their notable products is GEMFIBROZIL, with a corresponding application number 18422.

    Regulatory Information DISCN

    With a dosage strength 200MG

    Dosage Form Route CAPSULE; ORAL

    Reference Listed Drug No

    Approved since 1982-01-01

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