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Priya Life Science Medicines register
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Registers› Irish medicines
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.

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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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53 of 10,336 medicines
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Medicine
Active substance
Licence holder
Status
10 mg/ml Solution for infusion EU/1/19/1383/001-002
Lacosamide
UCB Pharma S.A.
—
Briviact 10 mg film-coated tablets EU/1/15/1073/001-004
Brivaracetam
UCB Pharma S.A.
—
Briviact 10 mg/ml oral solution EU/1/15/1073/021
Brivaracetam
UCB Pharma S.A.
—
Briviact 100 mg film-coated tablets EU/1/15/1073/017-020
Brivaracetam
UCB Pharma S.A.
—
Briviact 25 mg film-coated tablets EU/1/15/1073/005-008
Brivaracetam
UCB Pharma S.A.
—
Briviact 50 mg film-coated tablets EU/1/15/1073/009-012
Brivaracetam
UCB Pharma S.A.
—
Briviact 75 mg film-coated tablets EU/1/15/1073/013-016
Brivaracetam
UCB Pharma S.A.
—
Fintepla 2.2 mg/ml oral solution EU/1/20/1491/001-004
Fenfluramine hydrochloride
UCB Pharma S.A.
—
Keppra 100 mg/ml oral solution EU/1/00/146/027
Levetiracetam
UCB Pharma S.A.
—
Keppra 1000 mg film-coated tablets EU/1/00/146/020-026
Levetiracetam
UCB Pharma S.A.
—
Keppra 250 mg film-coated tablets EU/1/00/146/001-005
Levetiracetam
UCB Pharma S.A.
—
Keppra 500 mg film-coated tablets EU/1/00/146/006-013
Levetiracetam
UCB Pharma S.A.
—
Keppra 750 mg film-coated tablets EU/1/00/146/014-019
Levetiracetam
UCB Pharma S.A.
—
KYGEVVI 2 g/2 g powder for oral solution EU/1/25/2013/001
Doxecitine, Doxribtimine
UCB Pharma S.A.
—
Lacosamide UCB 10 mg/ml Syrup EU/1/19/1383/003
Lacosamide
UCB Pharma S.A.
—
Lacosamide UCB 100 mg Film-coated tablet EU/1/19/1383/010-015
Lacosamide
UCB Pharma S.A.
—
Lacosamide UCB 150 mg Film-coated tablet EU/1/19/1383/016-021
Lacosamide
UCB Pharma S.A.
—
Lacosamide UCB 200 mg Film-coated tablet EU/1/19/1383/022-027
Lacosamide
UCB Pharma S.A.
—
Lacosamide UCB 50 mg Film-coated tablet EU/1/19/1383/004-009
Lacosamide
UCB Pharma S.A.
—
Neupro EU/1/05/331/1-3,14-20
Rotigotine
UCB Pharma S.A.
—
Neupro EU/1/05/331/38-46
Rotigotine
UCB Pharma S.A.
—
Neupro EU/1/05/331/47-55
Rotigotine
UCB Pharma S.A.
—
Rystiggo 140 mg/ml solution for injection EU/1/23/1780/001
Rozanolixizumab
UCB Pharma S.A.
—
Tylex 30 mg/500 mg Hard Capsules PA0891/014/001
Codeine phosphate hemihydrate, Paracetamol
UCB (Pharma) Ireland Limited,
Marketed
Vimpat 10 mg/ml syrup EU/1/08/470/018-019
Lacosamide
UCB Pharma S.A.
—
Vimpat 100 mg film-coated tablets EU/1/08/470/4-6
Lacosamide
UCB Pharma S.A.
—
Vimpat 15 mg/ml syrup EU/1/08/470/14-15
Lacosamide
UCB Pharma S.A.
—
Vimpat 150 mg film-coated tablets EU/1/08/470/7-9
Lacosamide
UCB Pharma S.A.
—
Vimpat 200 mg film-coated tablets EU/1/08/470/10-12
Lacosamide
UCB Pharma S.A.
—
Vimpat 50 mg film-coated tablets EU/1/08/470/1-3
Lacosamide
UCB Pharma S.A.
—
Xyrem 500 mg/mL oral solution EU/1/05/312/001
Sodium Oxybate
UCB Pharma S.A.
—
Xyzal 0.5 mg/ml oral solution PA0891/003/003
Levocetirizine dihydrochloride
UCB (Pharma) Ireland Limited,
Marketed
Xyzal 5 mg film-coated tablets PA0891/003/001
Levocetirizine dihydrochloride
UCB (Pharma) Ireland Limited,
Marketed
Xyzal 5 mg/ml oral drops, solution PA0891/003/002
Levocetirizine dihydrochloride
UCB (Pharma) Ireland Limited,
Not marketed
Zirtek 1 mg/ml oral solution PA0891/008/003
Cetirizine dihydrochloride
UCB (Pharma) Ireland Limited,
Marketed
Zirtek 10 mg film-coated tablets PA0891/008/002
Cetirizine hydrochloride
UCB (Pharma) Ireland Limited,
Marketed
Showing 1–50 of 53
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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.