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    Fosinopril

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    01 4ANI Pharmaceuticals Inc

    02 9Actavis Inc

    03 2Alphapharm PTY Ltd

    04 7Apotex Inc

    05 14Aurobindo Pharma Limited

    06 2Aurovitas Spain, Sau

    07 2Bausch Health

    08 9Bristol Myers Squibb

    09 5Chartwell Pharmaceuticals llc

    10 4DOC Generici

    11 5InvaGen Pharmaceuticals Inc

    12 2MS Pharma

    13 1Medis ehff

    14 5Menarini

    15 1Mepha Pharma

    16 3PHARMASWISS CESKA REPUBL.S.R.O

    17 3PHARMASWISS CESKA REPUBLIKA SRO

    18 2Pharmascience Inc.

    19 3Prinston

    20 2SANIS HEALTH INC

    21 2Sandoz B2B

    22 5Sun Pharmaceutical Industries Limited

    23 12Teva Pharmaceutical Industries

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    01

    Actavis Inc

    Ireland
    Global ChemShow
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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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    ANI Pharmaceuticals Inc

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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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    Regulatory Info : DISCN

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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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    Regulatory Info : DISCN

    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
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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
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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

    Regulatory Info : DISCN

    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**

    Packaging :

    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
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    Bristol Myers Squibb

    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
    Global ChemShow
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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
    Global ChemShow
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    Regulatory Info : RX

    Registration Country : USA

    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
    Global ChemShow
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    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 : 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
    Global ChemShow
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    Global ChemShow
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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
    Global ChemShow
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    Sun Pharmaceutical Industries Limit...

    India
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    Global ChemShow
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    Regulatory Info : DISCN

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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
    Global ChemShow
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    Sun Pharmaceutical Industries Limit...

    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
    Global ChemShow
    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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    16

    Teva Pharmaceutical Industries

    Israel
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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
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    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
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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
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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 2004-10-08

    Application Number : 76188

    Regulatory Info : DISCN

    Registration Country : USA

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    Upsher-Smith Laboratories

    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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