Tecfidera

dimethyl fumarate · Biogen Netherlands B.V.
AUTHORISED IN THE EU

What Tecfidera is used for

Tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (RRMS).

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Tecfidera
Active substance
dimethyl fumarate
Disease area
Multiple Sclerosis
Medicine group
Immunosuppressants
ATC code
L04AX07
Marketing authorisation holder
Biogen Netherlands B.V.
Authorised in the EU since
2014

Official information

In India

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Tecfidera used for?

Tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (RRMS).

What is the active substance in Tecfidera?

Tecfidera contains dimethyl fumarate.

Who makes Tecfidera?

The EU marketing authorisation holder is Biogen Netherlands B.V..

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

← All specialty medicines, EU

For information only, not medical advice. This page is a plain-language summary written from standard prescribing information and the public guides linked below. Brands sometimes change their formula, so always check the composition printed on the pack. Doses here are typical adult doses; yours may differ. Do not start, stop or change a medicine without your doctor or pharmacist, and keep all medicines away from children. In an emergency, call 112 (India) or your local emergency number.