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    List of All Manufacturers & Suppliers of Fosinopril Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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

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    FAMAR CDMO- From early development to commercial manufacturing.

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    xyz-pharma-m-2024-09-09

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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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    Veranova: A CDMO that manages complexity with confidence.

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    xyz-pharma-m-2024-09-09

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    Fosinopril

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    DIGITAL CONTENT

    GLOBAL SALES INFORMATION

    MARKET PLACE

    PATENTS & EXCLUSIVITIES

    REF. STANDARDS & IMPURITIES

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    $ API Ref.Price (USD/KG) : 1,922Xls

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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 3RANBAXY LABORATORIES LIMITED

    19 2SANIS HEALTH INC

    20 2Sandoz B2B

    21 2Sun Pharmaceutical Industries Limited

    22 10Teva Pharmaceutical Industries

    23 3Upsher-Smith Laboratories

    24 8Viatris

    25 2Zentiva

    26 10Blank

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    01

    Actavis Inc

    Ireland
    BioProcess International
    Not Confirmed
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    Actavis Inc

    Ireland
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    BioProcess International
    Not Confirmed
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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 : 2004-10-15

    Application Number : 76620

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    ANI Pharmaceuticals Inc

    U.S.A
    BioProcess International
    Not Confirmed
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    ANI Pharmaceuticals Inc

    U.S.A
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    BioProcess International
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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 : 2004-12-03

    Application Number : 76608

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    ANI Pharmaceuticals Inc

    U.S.A
    BioProcess International
    Not Confirmed
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    ANI Pharmaceuticals Inc

    U.S.A
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    BioProcess International
    Not Confirmed
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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 : 20MG;12.5MG

    Packaging :

    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
    BioProcess International
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioProcess International
    Not Confirmed
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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**

    Packaging :

    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
    BioProcess International
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioProcess International
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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**

    Packaging :

    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
    BioProcess International
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioProcess International
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    BioProcess International
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioProcess International
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    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
    BioProcess International
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
    arrow
    BioProcess International
    Not Confirmed
    • fda
    • EDQM
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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
    BioProcess International
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
    arrow
    BioProcess International
    Not Confirmed
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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
    BioProcess International
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
    arrow
    BioProcess International
    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 : 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
    BioProcess International
    Not Confirmed
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    Chartwell Pharmaceuticals llc

    U.S.A
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    BioProcess International
    Not Confirmed
    • fda
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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

    RANBAXY LABORATORIES LIMITED

    India
    BioProcess International
    Not Confirmed
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    RANBAXY LABORATORIES LIMITED

    India
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    BioProcess International
    Not Confirmed
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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 : 2004-04-23

    Application Number : 76580

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    RANBAXY LABORATORIES LIMITED

    India
    BioProcess International
    Not Confirmed
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    RANBAXY LABORATORIES LIMITED

    India
    arrow
    BioProcess International
    Not Confirmed
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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

    RANBAXY LABORATORIES LIMITED

    India
    BioProcess International
    Not Confirmed
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    RANBAXY LABORATORIES LIMITED

    India
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    BioProcess International
    Not Confirmed
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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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    15

    Teva Pharmaceutical Industries

    Israel
    BioProcess International
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    BioProcess International
    Not Confirmed
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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 : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    16

    Teva Pharmaceutical Industries

    Israel
    BioProcess International
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    BioProcess International
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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 : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    17

    Teva Pharmaceutical Industries

    Israel
    BioProcess International
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    BioProcess International
    Not Confirmed
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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 : 2003-11-25

    Application Number : 76139

    Regulatory Info : RX

    Registration Country : USA

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    18

    Upsher-Smith Laboratories

    U.S.A
    BioProcess International
    Not Confirmed
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    Upsher-Smith Laboratories

    U.S.A
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    BioProcess International
    Not Confirmed
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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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    19

    Upsher-Smith Laboratories

    U.S.A
    BioProcess International
    Not Confirmed
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    Upsher-Smith Laboratories

    U.S.A
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    BioProcess International
    Not Confirmed
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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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    20

    Upsher-Smith Laboratories

    U.S.A
    BioProcess International
    Not Confirmed
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    Upsher-Smith Laboratories

    U.S.A
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    BioProcess International
    Not Confirmed
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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 : 2004-10-08

    Application Number : 76188

    Regulatory Info : DISCN

    Registration Country : USA

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