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    Trusted Global CDMO Partner Delivering End-to-End Pharma Manufacturing & Development Solutions.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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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

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    14 3PHARMASWISS CESKA REPUBL.S.R.O

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    17 3Prinston

    18 2SANIS HEALTH INC

    19 2Sandoz B2B

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    01

    Actavis Inc

    Ireland
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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

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    Approval Date : 2004-10-15

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    03

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    FOSINOPRIL SODIUM

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    Dosage Strength : 40MG

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    Approval Date : 2004-10-15

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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

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    Registration Country : USA

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    05

    ANI Pharmaceuticals Inc

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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

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    Apotex Inc

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    FOSINOPRIL SODIUM

    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2005-05-17

    Application Number : 76906

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    07

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    Brand Name : FOSINOPRIL SODIUM

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    Approval Date : 2005-05-17

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    Apotex Inc

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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 2005-05-17

    Application Number : 76906

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    09

    Bristol Myers Squibb

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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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    10

    Bristol Myers Squibb

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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

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    Registration Country : USA

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    11

    Bristol Myers Squibb

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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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    12

    Bristol Myers Squibb

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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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    13

    Bristol Myers Squibb

    U.S.A
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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**

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    Approval Date : 1994-11-30

    Application Number : 20286

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Chartwell Pharmaceuticals llc

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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

    Registration Country : USA

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    15

    Chartwell Pharmaceuticals llc

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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG

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    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

    Registration Country : USA

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    16

    Chartwell Pharmaceuticals llc

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    Chartwell Pharmaceuticals llc

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    Brand Name : FOSINOPRIL SODIUM

    Dosage Form : TABLET;ORAL

    Dosage Strength : 40MG

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    Approval Date : 2004-04-23

    Application Number : 76483

    Regulatory Info : RX

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    17

    Sandoz B2B

    Switzerland
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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 : 2005-09-28

    Application Number : 76961

    Regulatory Info : RX

    Registration Country : USA

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    18

    Sun Pharmaceutical Industries Limit...

    India
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    Sun Pharmaceutical Industries Limit...

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    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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    19

    Sun Pharmaceutical Industries Limit...

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    Sun Pharmaceutical Industries Limit...

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    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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    20

    Sun Pharmaceutical Industries Limit...

    India
    AAN
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    Regulatory Info : DISCN

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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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    21

    Sun Pharmaceutical Industries Limit...

    India
    AAN
    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG

    Packaging :

    Approval Date : 2004-12-17

    Application Number : 76739

    Regulatory Info : DISCN

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

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    Not Confirmed
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    Sun Pharmaceutical Industries Limit...

    India
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    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG

    Packaging :

    Approval Date : 2004-12-17

    Application Number : 76739

    Regulatory Info : DISCN

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
    AAN
    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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    24

    Teva Pharmaceutical Industries

    Israel
    AAN
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    AAN
    Not Confirmed
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    • EDQM
    • WHO-GMP
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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 : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    25

    Teva Pharmaceutical Industries

    Israel
    AAN
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    AAN
    Not Confirmed
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    • EDQM
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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 : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    26

    Teva Pharmaceutical Industries

    Israel
    AAN
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    AAN
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG;12.5MG

    Packaging :

    Approval Date : 2006-07-05

    Application Number : 76945

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Teva Pharmaceutical Industries

    Israel
    AAN
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    AAN
    Not Confirmed
    • fda
    • EDQM
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    Flag Israel
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    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE

    Brand Name : FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 20MG;12.5MG

    Packaging :

    Approval Date : 2006-07-05

    Application Number : 76945

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Upsher-Smith Laboratories

    U.S.A
    AAN
    Not Confirmed
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    Upsher-Smith Laboratories

    U.S.A
    arrow
    AAN
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    29

    Upsher-Smith Laboratories

    U.S.A
    AAN
    Not Confirmed
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    Upsher-Smith Laboratories

    U.S.A
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    AAN
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Virtual Booth Virtual Booth
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    Regulatory Info : DISCN

    Registration Country : USA

    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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    30

    Upsher-Smith Laboratories

    U.S.A
    AAN
    Not Confirmed
    arrow

    Upsher-Smith Laboratories

    U.S.A
    arrow
    AAN
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Virtual Booth Virtual Booth
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    Regulatory Info : DISCN

    Registration Country : USA

    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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