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    Fosinopril

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    03 2Alphapharm PTY Ltd

    04 7Apotex Inc

    05 10Aurobindo Pharma Limited

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    07 8Bristol Myers Squibb

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    01

    Actavis Inc

    Ireland
    APGA Annual Conference
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    Regulatory Info : DISCN

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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2004-10-15

    Application Number : 76620

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    ANI Pharmaceuticals Inc

    U.S.A
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    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG

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    Approval Date : 2004-12-03

    Application Number : 76608

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    ANI Pharmaceuticals Inc

    U.S.A
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    U.S.A
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    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG

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    Approval Date : 2004-12-03

    Application Number : 76608

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Bristol Myers Squibb

    U.S.A
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    Registration Country : USA

    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1991-05-16

    Application Number : 19915

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Bristol Myers Squibb

    U.S.A
    APGA Annual Conference
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    U.S.A
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    Regulatory Info : DISCN

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    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

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

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    Approval Date : 1991-05-16

    Application Number : 19915

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Bristol Myers Squibb

    U.S.A
    APGA Annual Conference
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    U.S.A
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    FOSINOPRIL SODIUM

    Brand Name : MONOPRIL

    Dosage Form : TABLET;ORAL

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

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    Approval Date : 1995-03-28

    Application Number : 19915

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    Registration Country : USA

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    07

    Bristol Myers Squibb

    U.S.A
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    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : MONOPRIL-HCT

    Dosage Form : TABLET;ORAL

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

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    Approval Date : 1994-11-30

    Application Number : 20286

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Bristol Myers Squibb

    U.S.A
    APGA Annual Conference
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    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : MONOPRIL-HCT

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1994-11-30

    Application Number : 20286

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Chartwell Pharmaceuticals llc

    U.S.A
    APGA Annual Conference
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    Chartwell Pharmaceuticals llc

    U.S.A
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    Regulatory Info : RX

    Registration Country : USA

    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

    Registration Country : USA

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    10

    Chartwell Pharmaceuticals llc

    U.S.A
    APGA Annual Conference
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    U.S.A
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    Regulatory Info : RX

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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

    Registration Country : USA

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    11

    Chartwell Pharmaceuticals llc

    U.S.A
    APGA Annual Conference
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    U.S.A
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    Regulatory Info : RX

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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

    Registration Country : USA

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    12

    Sun Pharmaceutical Industries Limit...

    India
    APGA Annual Conference
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    APGA Annual Conference
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76580

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Sun Pharmaceutical Industries Limit...

    India
    APGA Annual Conference
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    APGA Annual Conference
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76580

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Sun Pharmaceutical Industries Limit...

    India
    APGA Annual Conference
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    India
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2004-04-23

    Application Number : 76580

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Teva Pharmaceutical Industries

    Israel
    APGA Annual Conference
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
    APGA Annual Conference
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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    17

    Teva Pharmaceutical Industries

    Israel
    APGA Annual Conference
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    18

    Upsher-Smith Laboratories

    U.S.A
    APGA Annual Conference
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2004-10-08

    Application Number : 76188

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Upsher-Smith Laboratories

    U.S.A
    APGA Annual Conference
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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2004-10-08

    Application Number : 76188

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    Registration Country : USA

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    Upsher-Smith Laboratories

    U.S.A
    APGA Annual Conference
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    U.S.A
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 2004-10-08

    Application Number : 76188

    Regulatory Info : DISCN

    Registration Country : USA

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