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

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Meclofenamic Acid

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 2A&M Therapy

    02 2ANI Pharmaceuticals Inc

    03 4Actavis Inc

    04 2Barr Laboratories

    05 2Chartwell Pharmaceuticals llc

    06 2Menarini

    07 1PHARMAFAR Srl

    08 2Par Pharmaceutical

    09 2Pfizer Inc

    10 2QUANTUM PHARMICS

    11 2USL PHARMA

    12 2VITARINE

    13 2Viatris

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    01

    A&M Therapy

    U.S.A
    Discovery on Target
    Not Confirmed
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    A&M Therapy

    U.S.A
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    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-02-10

    Application Number : 71362

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    A&M Therapy

    U.S.A
    Discovery on Target
    Not Confirmed
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    A&M Therapy

    U.S.A
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    Discovery on Target
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1987-02-10

    Application Number : 71363

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
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    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1986-11-25

    Application Number : 70400

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
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    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1986-11-25

    Application Number : 70401

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-08-11

    Application Number : 71640

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Actavis Inc

    Ireland
    Discovery on Target
    Not Confirmed
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    Actavis Inc

    Ireland
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1987-08-11

    Application Number : 71641

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    ANI Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    ANI Pharmaceuticals Inc

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

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1987-04-15

    Application Number : 71469

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    ANI Pharmaceuticals Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    ANI Pharmaceuticals Inc

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

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-04-15

    Application Number : 71469

    Regulatory Info : DISCN

    Registration Country : USA

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    Portfolio PDF

    Product Web Link

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    09

    Par Pharmaceutical

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Par Pharmaceutical

    U.S.A
    arrow
    Discovery on Target
    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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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-03-10

    Application Number : 72077

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Par Pharmaceutical

    U.S.A
    Discovery on Target
    Not Confirmed
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    Par Pharmaceutical

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-03-10

    Application Number : 72078

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Pfizer Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Pfizer Inc

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOMEN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18006

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Pfizer Inc

    U.S.A
    Discovery on Target
    Not Confirmed
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    Pfizer Inc

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

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOMEN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18006

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    USL PHARMA

    United Kingdom
    Discovery on Target
    Not Confirmed
    arrow

    USL PHARMA

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-03-25

    Application Number : 71007

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    USL PHARMA

    United Kingdom
    Discovery on Target
    Not Confirmed
    arrow

    USL PHARMA

    United Kingdom
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-03-25

    Application Number : 71008

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Viatris

    U.S.A
    Discovery on Target
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1986-09-03

    Application Number : 71081

    Regulatory Info : RX

    Registration Country : USA

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    16

    Viatris

    U.S.A
    Discovery on Target
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
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    Regulatory Info : RX

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1986-09-03

    Application Number : 71081

    Regulatory Info : RX

    Registration Country : USA

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    17

    QUANTUM PHARMICS

    Country
    Discovery on Target
    Not Confirmed
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    QUANTUM PHARMICS

    Country
    arrow
    Discovery on Target
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1987-07-14

    Application Number : 71380

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    QUANTUM PHARMICS

    Country
    Discovery on Target
    Not Confirmed
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    QUANTUM PHARMICS

    Country
    arrow
    Discovery on Target
    Not Confirmed
    • fda
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1987-07-14

    Application Number : 71381

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    VITARINE

    Country
    Discovery on Target
    Not Confirmed
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    VITARINE

    Country
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 100MG BASE

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 71684

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    VITARINE

    Country
    Discovery on Target
    Not Confirmed
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    VITARINE

    Country
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    MECLOFENAMATE SODIUM

    Brand Name : MECLOFENAMATE SODIUM

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : EQ 50MG BASE

    Packaging :

    Approval Date : 1988-06-15

    Application Number : 71710

    Regulatory Info : DISCN

    Registration Country : USA

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