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    Approved Drug Products containing 76467 listed in the FDA Orange Book. Original Data : FDA Website

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    Actavis Inc

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    01 WATSON LABS (3)

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    01 TABLET, EXTENDED RELEASE;ORAL (3)

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    01 GLIPIZIDE (3)

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    01 No (3)

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    GLIPIZIDE

    PDF Supplier PDF
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    TABLET, EXTENDED R...
    10MG
    2003-11-07
    76467
    GLIPIZIDE
    RX
    No
    AB
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    GLIPIZIDE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET, EXTENDED R...
    2.5MG
    2006-03-27
    76467
    GLIPIZIDE
    RX
    No
    AB
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    • EDQM
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    GLIPIZIDE

    PDF Supplier PDF
    URL Supplier Web Content
    TABLET, EXTENDED R...
    5MG
    2003-09-08
    76467
    GLIPIZIDE
    RX
    No
    AB
    ASK
    US
    PHARMACOMPASS
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    Looking for FDA Orange Book APPLICATION 76467

    Looking for FDA Orange Book APPLICATION 76467 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 GLIPIZIDE, with a corresponding application number 76467.

    Regulatory Information RX

    With a dosage strength 10MG

    Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2003-11-07

    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 GLIPIZIDE, with a corresponding application number 76467.

    Regulatory Information RX

    With a dosage strength 2.5MG

    Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2006-03-27

    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 GLIPIZIDE, with a corresponding application number 76467.

    Regulatory Information RX

    With a dosage strength 5MG

    Dosage Form Route TABLET, EXTENDED RELEASE; ORAL

    Reference Listed Drug No

    Approved since 2003-09-08

    Therapeutic Equivalence (TE) Code AB

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