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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Moexipril

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    Apotex Inc

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2008-06-02

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Avet 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 : 2014-03-07

    Application Number : 202150

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG

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    Approval Date : 2014-03-07

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    Avet Pharmaceuticals

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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 : 2014-03-07

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    Chartwell Pharmaceuticals llc

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

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    Approval Date : 2006-11-30

    Application Number : 77536

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    Registration Country : USA

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    Chartwell Pharmaceuticals llc

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

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    Approval Date : 2006-11-30

    Application Number : 77536

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    Registration Country : USA

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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

    Packaging :

    Approval Date : 2008-09-25

    Application Number : 90096

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Chartwell Pharmaceuticals llc

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG

    Packaging :

    Approval Date : 2008-09-25

    Application Number : 90096

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Chartwell Pharmaceuticals llc

    U.S.A
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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG

    Packaging :

    Approval Date : 2008-09-25

    Application Number : 90096

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Glenmark Pharmaceuticals

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2010-03-30

    Application Number : 90416

    Regulatory Info : RX

    Registration Country : USA

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    12

    Glenmark Pharmaceuticals

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    Regulatory Info : RX

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2010-03-30

    Application Number : 90416

    Regulatory Info : RX

    Registration Country : USA

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    13

    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

    Packaging :

    Approval Date : 2010-03-17

    Application Number : 90718

    Regulatory Info : RX

    Registration Country : USA

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    14

    Glenmark Pharmaceuticals

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;15MG

    Packaging :

    Approval Date : 2010-03-17

    Application Number : 90718

    Regulatory Info : RX

    Registration Country : USA

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    Glenmark Pharmaceuticals

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;15MG

    Packaging :

    Approval Date : 2010-03-17

    Application Number : 90718

    Regulatory Info : RX

    Registration Country : USA

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    Meda Pharmaceuticals Inc.

    U.S.A
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    Registration Country : Italy

    Moexipril; Hydrochlorothiazide

    Brand Name : Enulid

    Dosage Form : Moexipril+Hydrochlorothiazide 25+15Mg 14 Joined' Oral Use

    Dosage Strength : 14 cpr riv 15 mg + 25 mg

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    Registration Country : Italy

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    Teva Pharmaceutical Industries

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 7.5MG

    Packaging :

    Approval Date : 2003-05-08

    Application Number : 76204

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

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    MOEXIPRIL HYDROCHLORIDE

    Brand Name : MOEXIPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2003-05-08

    Application Number : 76204

    Regulatory Info : RX

    Registration Country : USA

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    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

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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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

    Regulatory Info : RX

    Registration Country : USA

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    HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE

    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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    Regulatory Info : DISCN

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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**

    Packaging :

    Approval Date : 1995-04-19

    Application Number : 20312

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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    MOEXIPRIL HYDROCHLORIDE

    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**

    Packaging :

    Approval Date : 1995-04-19

    Application Number : 20312

    Regulatory Info : DISCN

    Registration Country : USA

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    UCB Pharma S.A

    Belgium
    Fi Europe 2024
    Not Confirmed
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    UCB Pharma S.A

    Belgium
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    Fi Europe 2024
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 1997-06-27

    Application Number : 20729

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    UCB Pharma S.A

    Belgium
    Fi Europe 2024
    Not Confirmed
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    Belgium
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    26

    UCB Pharma S.A

    Belgium
    Fi Europe 2024
    Not Confirmed
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    UCB Pharma S.A

    Belgium
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    Fi Europe 2024
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    Approval Date : 2002-02-14

    Application Number : 20729

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    UCB Pharma S.A

    Belgium
    Fi Europe 2024
    Not Confirmed
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    UCB Pharma S.A

    Belgium
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    Fi Europe 2024
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    Regulatory Info :

    Registration Country : Italy

    Moexipril

    Brand Name : Femipres

    Dosage Form : Moexipril 15Mg 14 Joined' Oral Use

    Dosage Strength : 14 cpr riv 15 mg

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    28

    UCB Pharma S.A

    Belgium
    Fi Europe 2024
    Not Confirmed
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    UCB Pharma S.A

    Belgium
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    Fi Europe 2024
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    Regulatory Info :

    Registration Country : Italy

    Moexipril; Hydrochlorothiazide

    Brand Name : Femipres Plus

    Dosage Form : Moexipril+Hydrochlorothiazide 25+15Mg 14 Joined' Oral Use

    Dosage Strength : 14 cpr riv 15 mg + 25 mg

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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