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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    Inke S.A: APIs manufacturing plant.

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    Fosinopril

    ACTIVE PHARMA INGREDIENTS

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    01 4ANI Pharmaceuticals Inc

    02 15Actavis Inc

    03 2Alphapharm PTY Ltd

    04 7Apotex Inc

    05 10Aurobindo Pharma Limited

    06 2Avet Pharmaceuticals

    07 8Bristol Myers Squibb

    08 3Chartwell Pharmaceuticals llc

    09 4DOC Generici

    10 5InvaGen Pharmaceuticals Inc

    11 2MS Pharma

    12 5Menarini

    13 2Mepha Pharma

    14 3PHARMASWISS CESKA REPUBL.S.R.O

    15 3PHARMASWISS CESKA REPUBLIKA SRO

    16 2Pharmascience Inc.

    17 3Prinston

    18 2SANIS HEALTH INC

    19 2Sandoz B2B

    20 5Sun Pharmaceutical Industries Limited

    21 10Teva Pharmaceutical Industries

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    01

    Actavis Inc

    Ireland
    Iran Expo
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    Regulatory Info : DISCN

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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    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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    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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    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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    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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    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**

    Packaging :

    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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    U.S.A
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    Regulatory Info : DISCN

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    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
    Iran Expo
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    Chartwell Pharmaceuticals llc

    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 : 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
    Iran Expo
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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
    Iran Expo
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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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
    Iran Expo
    Not Confirmed
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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 : 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
    Iran Expo
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    Iran Expo
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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
    Iran Expo
    Not Confirmed
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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
    Iran Expo
    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

    Packaging :

    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
    Iran Expo
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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
    Iran Expo
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    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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    20

    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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