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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    quinapril hydrochloride hydrochloride

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    01 2Aspen Pharmacare Holdings

    02 4ANI Pharmaceuticals Inc

    03 8Actavis Inc

    04 2Adcock Ingram

    05 9Apotex Inc

    06 1Arrow Pharmaceuticals

    07 9Aurobindo Pharma Limited

    08 2Aurogen South Africa (Pty) Ltd

    09 1Aurovitas Spain, Sau

    10 1BENEDETTI & CO.SpA

    11 7Chartwell Pharmaceuticals llc

    12 3Cinfa

    13 2Daiichi Sankyo

    14 2EG SpA

    15 2EG Spa

    16 7InvaGen Pharmaceuticals Inc

    17 2LABORATORIOS NORMON SA

    18 4Lacer

    19 4Lupin Ltd

    20 3MALESCI SpA IST.FARMACOBIOL.

    21 2Malesci Istituto Farmacobiologico

    22 3Menarini

    23 2Novagen Pharma

    24 7PHARMOBEDIENT

    25 21Pfizer Inc

    26 4Pharma Dynamics

    27 4Pharmascience Inc.

    28 4Prinston

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    30 3Sandoz B2B

    31 11Sun Pharmaceutical Industries Limited

    32 3Tamarang

    33 10Viatris

    34 5Zentiva

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    01

    Aspen Pharmacare Holdings

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    Regulatory Info : Generic

    Registration Country : South Africa

    Quinapril

    Brand Name : Quinaspen

    Dosage Form : TAB

    Dosage Strength : 20mg

    Packaging : 30X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Africa

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    02

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : Generic

    Registration Country : South Africa

    Quinapril

    Brand Name : Quinaspen 10 mg

    Dosage Form : TAB

    Dosage Strength : 10mg

    Packaging : 30X1mg

    Approval Date :

    Application Number :

    Regulatory Info : Generic

    Registration Country : South Africa

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    03

    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 2005-01-14

    Application Number : 76049

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Actavis Inc

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 2005-01-14

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    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Actavis Inc

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

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    Approval Date : 2005-01-14

    Application Number : 76049

    Regulatory Info : DISCN

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    06

    ANI Pharmaceuticals Inc

    U.S.A
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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2007-08-24

    Application Number : 75504

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    ANI Pharmaceuticals Inc

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 2007-08-24

    Application Number : 75504

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    ANI Pharmaceuticals Inc

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    Regulatory Info : DISCN

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2007-08-24

    Application Number : 75504

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    ANI Pharmaceuticals Inc

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2007-08-24

    Application Number : 75504

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Pfizer Inc

    U.S.A
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    Pfizer Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-19

    Application Number : 19885

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Pfizer Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-19

    Application Number : 19885

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Pfizer Inc

    U.S.A
    ASPEN
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    Regulatory Info : DISCN

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-19

    Application Number : 19885

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Pfizer Inc

    U.S.A
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    Regulatory Info : DISCN

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCUPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1991-11-19

    Application Number : 19885

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Pfizer Inc

    U.S.A
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    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1999-12-28

    Application Number : 20125

    Regulatory Info : DISCN

    Registration Country : USA

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    Pfizer Inc

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    Regulatory Info : DISCN

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    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 12.5MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1999-12-28

    Application Number : 20125

    Regulatory Info : DISCN

    Registration Country : USA

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    Pfizer Inc

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    HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE

    Brand Name : ACCURETIC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG;EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1999-12-28

    Application Number : 20125

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    Viatris

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 2005-01-28

    Application Number : 76036

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    Viatris

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    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 2005-01-28

    Application Number : 76036

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    Registration Country : USA

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    19

    Viatris

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    QUINAPRIL HYDROCHLORIDE

    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Packaging :

    Approval Date : 2005-01-28

    Application Number : 76036

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    Viatris

    U.S.A
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    Brand Name : QUINAPRIL HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Packaging :

    Approval Date : 2005-01-28

    Application Number : 76036

    Regulatory Info : DISCN

    Registration Country : USA

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