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    MOEXIPRIL HYDROCHLORIDE

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    MOEXIPRIL HYDROCHLORIDE

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    Approval Date : 2006-11-30

    Application Number : 77536

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    Chartwell Pharmaceuticals llc

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG

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    Approval Date : 2008-09-25

    Application Number : 90096

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    Chartwell Pharmaceuticals llc

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

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    Dosage Form : TABLET;ORAL

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    Approval Date : 2008-09-25

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    Chartwell Pharmaceuticals llc

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG

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    Approval Date : 2008-09-25

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    Glenmark Pharmaceuticals

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    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

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    Approval Date : 2010-03-30

    Application Number : 90416

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    09

    Glenmark Pharmaceuticals

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    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2010-03-30

    Application Number : 90416

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    10

    Glenmark Pharmaceuticals

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG

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    Approval Date : 2010-03-17

    Application Number : 90718

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    11

    Teva Pharmaceutical Industries

    Israel
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    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

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    Approval Date : 2003-05-08

    Application Number : 76204

    Regulatory Info : RX

    Registration Country : USA

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    12

    Teva Pharmaceutical Industries

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    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2003-05-08

    Application Number : 76204

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    13

    Teva Pharmaceutical Industries

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG

    Packaging :

    Approval Date : 2007-03-07

    Application Number : 76980

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    Registration Country : USA

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    Teva Pharmaceutical Industries

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    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG

    Packaging :

    Approval Date : 2007-03-07

    Application Number : 76980

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    Registration Country : USA

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    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG

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    Approval Date : 2007-03-07

    Application Number : 76980

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    UCB Pharma S.A

    Belgium
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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIVASC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1995-04-19

    Application Number : 20312

    Regulatory Info : DISCN

    Registration Country : USA

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    UCB Pharma S.A

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    Brand Name : UNIVASC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1995-04-19

    Application Number : 20312

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    Registration Country : USA

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    UCB Pharma S.A

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;7.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1997-06-27

    Application Number : 20729

    Regulatory Info : DISCN

    Registration Country : USA

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    UCB Pharma S.A

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1997-06-27

    Application Number : 20729

    Regulatory Info : DISCN

    Registration Country : USA

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    UCB Pharma S.A

    Belgium
    STLE Annual Meeting
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : UNIRETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2002-02-14

    Application Number : 20729

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    Registration Country : USA

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