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Medicines register · Ireland

Every medicine authorised for the Irish market

The Health Products Regulatory Authority's full list of authorised products — brand, active substance, licence holder, licence number and market status. Filter it, cite it, and take it away as a file.

Source: HPRA open dataset ("Authorised or Transfer Pending Products"), CC BY 4.0. Complete coverage — all 10,336 authorised products are in this register. Synced 20 Sep 2026, 17:51 UTC

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Matches brand name, active substance, licence holder and licence number.

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Medicine

Active substance

Licence holder

Status

AVONEX 30 micrograms/0.5 ml solution for injection. EU/1/97/033/003

Interferon beta - 1a

Biogen Netherlands B.V.

—

Plegridy EU/1/14/934/002

Peginterferon beta-1a

Biogen Netherlands B.V.

—

Plegridy 125 micrograms solution for injection in pre-filled pen EU/1/14/934/005-006

Peginterferon beta-1a

Biogen Netherlands B.V.

—

Plegridy 125 micrograms solution for injection in pre-filled syringe EU/1/14/934/003-004

Peginterferon beta-1a

Biogen Netherlands B.V.

—

Plegridy 63 micrograms solution for injection in pre-filled syringe EU/1/14/934/001-002

Peginterferon beta-1a

Biogen Netherlands B.V.

—

Qalsody 100 mg solution for injection EU/1/23/1783/001

Tofersen

Biogen Netherlands B.V.

—

Skyclarys 50 mg hard capsules EU/1/23/1786/001-002

Omaveloxolone

Biogen Netherlands B.V.

—

Spinraza 12 mg solution for injection EU/1/17/1188/001

Nusinersen

Biogen Netherlands B.V.

—

Spinraza 28 mg solution for injection EU/1/17/1188/002

Nusinersen sodium

Biogen Netherlands B.V.

—

Spinraza 50 mg solution for injection EU/1/17/1188/003

Nusinersen sodium

Biogen Netherlands B.V.

—

Tecfidera 120 mg gastro-resistant hard capsules EU/1/13/837/001

Dimethyl Fumarate

Biogen Netherlands B.V.

—

Tecfidera 240 mg gastro-resistant hard capsules EU/1/13/837/002

Dimethyl Fumarate

Biogen Netherlands B.V.

—

Tysabri 150 mg solution for injection in pre-filled syringe EU/1/06/346/002

Natalizumab

Biogen Netherlands B.V.

—

Tysabri 300 mg concentrate for solution for infusion EU/1/06/346/001

Natalizumab

Biogen Netherlands B.V.

—

Vumerity 231 mg gastro-resistant hard capsules EU/1/21/1585/001-002

Diroximel Fumarate

Biogen Netherlands B.V.

—

Zurzuvae 20 mg hard capsules EU/1/25/1977/001-003

Zuranolone

Biogen Netherlands B.V.

—

Zurzuvae 25 mg hard capsules EU/1/25/1977/004-006

Zuranolone

Biogen Netherlands B.V.

—

Zurzuvae 30 mg hard capsules EU/1/25/1977/007

Zuranolone

Biogen Netherlands B.V.

—

Cite this view

Priya Life Science (2026). Irish Medicines Register, filtered. Derived from the HPRA open dataset. Retrieved 28 September 2026. https://priyalifescience.com/medicines

Download this register

GET /api/export.php?register=medicines-ie&format=csv Try the JSON export →

Regulatory information only — not medical advice. For the authoritative record see the HPRA register directly.