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

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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    Mycophenolate Sodium

    ACTIVE PHARMA INGREDIENTS

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    01 2ACCORD HLTHCARE

    02 2ALKEM LABS LTD

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    04 2APOTEX INC

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    06 4BIOCON PHARMA

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    01

    ACCORD HLTHCARE

    United Kingdom
    Antibody Engineering
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    ACCORD HLTHCARE

    United Kingdom
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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Approval Date : 2017-08-23

    Application Number : 202555

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    ACCORD HLTHCARE

    United Kingdom
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    ACCORD HLTHCARE

    United Kingdom
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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Approval Date : 2017-08-23

    Application Number : 202555

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    APOTEX INC

    Canada
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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Approval Date : 2012-08-21

    Application Number : 91558

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    APOTEX INC

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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Approval Date : 2014-08-19

    Application Number : 91558

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    NOVARTIS

    Switzerland
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    NOVARTIS

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    RLD : Yes

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYFORTIC

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Approval Date : 2004-02-27

    Application Number : 50791

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    06

    NOVARTIS

    Switzerland
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    RLD : Yes

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYFORTIC

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Approval Date : 2004-02-27

    Application Number : 50791

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    07

    RK PHARMA

    U.S.A
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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Approval Date : 2014-01-08

    Application Number : 91248

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    RK PHARMA

    U.S.A
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    RK PHARMA

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    RLD : No

    TE Code : AB

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Approval Date : 2014-01-08

    Application Number : 91248

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    TEVA PHARMS USA

    Israel
    Antibody Engineering
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    TEVA PHARMS USA

    Israel
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    RLD : No

    TE Code :

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 180MG BASE

    Approval Date : 2014-10-30

    Application Number : 202720

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    TEVA PHARMS USA

    Israel
    Antibody Engineering
    Not Confirmed
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    TEVA PHARMS USA

    Israel
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code :

    MYCOPHENOLIC SODIUM

    Brand Name : MYCOPHENOLIC SODIUM

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : EQ 360MG BASE

    Approval Date : 2014-10-30

    Application Number : 202720

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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