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https://www.indianpharmapost.com/drug-approval/zydus-receives-fda-final-approval-for-diroximel-fumarate-delayed-release-capsules-231-mg-18228

INDPHARMAPOST
14 Nov 2025

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218596

FDA
12 Nov 2025

https://www.businesswire.com/news/home/20221013005410/en

BUSINESSWIRE
13 Oct 2022

http://www.pharmafile.com/news/606044/smc-approves-diroximel-fumarate-multiple-sclerosis-treatment

PHARMAFILE
08 Feb 2022
MHRA authorises Vumerity for multiple sclerosis patients
MHRA authorises Vumerity for multiple sclerosis patients

19 Nov 2021

// Lucy Parsons PHARMATIMES

https://www.pharmatimes.com/news/mhra_authorises_vumerity_for_multiple_sclerosis_patients_1383757

Lucy Parsons PHARMATIMES
19 Nov 2021
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