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    Approved Drug Products containing Alpharma brand of moexipril hydrochloride listed in the FDA Orange Book. Original Data : FDA Website

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    Alpharma brand of moexipril hydrochloride

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    01 APOTEX INC (2)

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    01 TABLET;ORAL (25)

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    01 DISCN (11)

    02 RX (14)

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    01 MOEXIPRIL HYDROCHLORIDE (8)

    02 MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (12)

    03 UNIRETIC (3)

    04 UNIVASC (2)

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    MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    7.5MG
    2003-05-08
    76204
    MOEXIPRIL HYDROCHLORID...
    RX
    No
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    MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    15MG
    2003-05-08
    76204
    MOEXIPRIL HYDROCHLORID...
    RX
    No
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    12.5MG;7.5MG
    2007-03-07
    76980
    MOEXIPRIL HYDROCHLORID...
    RX
    No
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    25MG;15MG
    2007-03-07
    76980
    MOEXIPRIL HYDROCHLORID...
    RX
    No
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    12.5MG;15MG
    2007-03-07
    76980
    MOEXIPRIL HYDROCHLORID...
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    No
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    MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
    1995-04-19
    20312
    UNIVASC
    DISCN
    No
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    MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
    1995-04-19
    20312
    UNIVASC
    DISCN
    No
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
    1997-06-27
    20729
    UNIRETIC
    DISCN
    No
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
    1997-06-27
    20729
    UNIRETIC
    DISCN
    No
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    UCB INC

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    TABLET;ORAL
    12.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
    2002-02-14
    20729
    UNIRETIC
    DISCN
    No
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