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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    FAMAR CDMO- From early development to commercial manufacturing.

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Mycophenolate Sodium

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    01 2Accord healthcare

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    07 2Concord Biotech

    08 2Fosun Wanbang Pharmaceutical

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    Accord healthcare

    United Kingdom
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2017-08-23

    Application Number : 202555

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    Accord healthcare

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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2017-08-23

    Application Number : 202555

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    03

    Alkem Laboratories

    India
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2021-09-23

    Application Number : 208315

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    Alkem Laboratories

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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2021-09-23

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    05

    Apotex Inc

    Canada
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2012-08-21

    Application Number : 91558

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    Apotex Inc

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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2014-08-19

    Application Number : 91558

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    Biocon

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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2021-11-29

    Application Number : 214630

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    Registration Country : USA

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    Biocon

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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2021-11-29

    Application Number : 214630

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    Registration Country : USA

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    09

    Concord Biotech

    India
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    Concord Biotech

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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Packaging :

    Approval Date : 2019-12-13

    Application Number : 211173

    Regulatory Info : RX

    Registration Country : USA

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    10

    Concord Biotech

    India
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Packaging :

    Approval Date : 2019-12-13

    Application Number : 211173

    Regulatory Info : RX

    Registration Country : USA

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    11

    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    MYCOPHENOLATE SODIUM

    Brand Name : MYFORTIC

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2004-02-27

    Application Number : 50791

    Regulatory Info : RX

    Registration Country : USA

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    12

    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    MYCOPHENOLATE SODIUM

    Brand Name : MYFORTIC

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2004-02-27

    Application Number : 50791

    Regulatory Info : RX

    Registration Country : USA

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    13

    RK Pharma

    U.S.A
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Packaging :

    Approval Date : 2014-01-08

    Application Number : 91248

    Regulatory Info : RX

    Registration Country : USA

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    14

    RK Pharma

    U.S.A
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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Packaging :

    Approval Date : 2014-01-08

    Application Number : 91248

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    Registration Country : USA

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    15

    Teva Pharmaceutical Industries

    Israel
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    Israel
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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Packaging :

    Approval Date : 2014-10-30

    Application Number : 202720

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Teva Pharmaceutical Industries

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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2014-10-30

    Application Number : 202720

    Regulatory Info : DISCN

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    17

    TWi Pharmaceuticals

    Taiwan
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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

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    Approval Date : 2021-11-03

    Application Number : 214289

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    TWi Pharmaceuticals

    Taiwan
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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

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    Approval Date : 2021-11-03

    Application Number : 214289

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    Yichang Humanwell Pharmaceutical

    China
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    China
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    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Packaging :

    Approval Date : 2021-02-10

    Application Number : 214376

    Regulatory Info : RX

    Registration Country : USA

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    Yichang Humanwell Pharmaceutical

    China
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    MYCOPHENOLATE SODIUM

    Brand Name : MYCOPHENOLATE SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Packaging :

    Approval Date : 2021-02-10

    Application Number : 214376

    Regulatory Info : RX

    Registration Country : USA

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