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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Monomethyl Fumarate

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    European Commission grants marketing authorisation for Vumerity
    European Commission grants marketing authorisation for Vumerity

    17 Nov 2021

    // Anna Begley EUROPEANPHARMACEUTICALREVIEW

    https://www.europeanpharmaceuticalreview.com/news/165570/european-commission-grants-marketing-authorisation-for-vumerity/

    Anna Begley EUROPEANPHARMACEUTICALREVIEW
    17 Nov 2021
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    Banner Life Sciences Announces BAFIERTAM, a Novel Oral Fumarate Treatment
    Banner Life Sciences Announces BAFIERTAM, a Novel Oral Fumarate Treatment

    03 Sep 2020

    // PRESS RELEASE

    https://www.pharmacompass.com/pdf/news/banner-life-sciences-announces-bafiertam-a-novel-oral-fumarate-treatment-1600067525.pdf

    PRESS RELEASE
    03 Sep 2020
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    Banner Life Sciences Announces Commercial Launch of BAFIERTAM
    Banner Life Sciences Announces Commercial Launch of BAFIERTAM

    16 Jul 2020

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20200716006004/en

    BUSINESSWIRE
    16 Jul 2020
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    Banner Life Sciences Announces Final FDA Approval of BAFIERTAM for MS
    Banner Life Sciences Announces Final FDA Approval of BAFIERTAM for MS

    01 May 2020

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20200430005256/en/Banner-Life-Sciences-Announces-Final-FDA-Approval

    BUSINESSWIRE
    01 May 2020
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    Banner Life Sciences Announces Final FDA Approval of BAFIERTAM for MS
    Banner Life Sciences Announces Final FDA Approval of BAFIERTAM for MS

    30 Apr 2020

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20200430005256/en

    BUSINESSWIRE
    30 Apr 2020
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    Alkermes and Biogen announce new MS drug application for FDA
    Alkermes and Biogen announce new MS drug application for FDA

    18 Dec 2018

    // Anna Smith PHARMA TIMES

    http://www.pharmatimes.com/news/alkermes_and_biogen_announce_new_ms_drug_application_for_fda_1272962

    Anna Smith PHARMA TIMES
    18 Dec 2018
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