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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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A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0–9
223 of 10,336 medicines
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Medicine
Active substance
Licence holder
Status
Jakavi EU/1/12/773/001
Ruxolitinib
Novartis Europharm Limited
—
Jakavi EU/1/12/773/002
Ruxolitinib
Novartis Europharm Limited
—
Jakavi 10 mg tablets EU/1/12/773/013-016
Ruxolitinib
Novartis Europharm Limited
—
Jakavi 20 mg tablets EU/1/12/773/003
Ruxolitinib
Novartis Europharm Limited
—
Jakavi 5 mg tablets EU/1/12/773/004-006
Ruxolitinib phosphate
Novartis Europharm Limited
—
Jakavi 5mg/ml Oral solution EU/1/12/773/017
Ruxolitinib phosphate
Novartis Europharm Limited
—
Jalra 50 mg tablets EU/1/08/485/1-11
Vildagliptin
Novartis Europharm Limited
—
Kymriah 1.2 × 106 – 6 × 108 cells dispersion for infusion EU/1/18/1297/001
AUTOGLAS T CELLS TRANSDUCED WITH LENTIVIRAL VECTOR CONTAINING A CHIMERIC ANTIGEN RECEPTOR DIRECTED AGAINST CD1
Novartis Europharm Limited
—
Lamisil 250 mg tablets PA0896/015/001
Terbinafine
Novartis Ireland Limited
Not marketed
Lioresal 10 mg Tablets PA0896/017/001
Baclofen
Novartis Ireland Limited
Marketed
Lioresal 5mg/5ml Oral solution PA0896/017/002
Baclofen
Novartis Ireland Limited
Marketed
Lutathera 370 MBq/mL solution for infusion EU/1/17/1226/001
177lu-dotao-tyr3-octeeotate
Novartis Europharm Limited
—
LysaKare 25 g/25 g Solution for infusion EU/1/19/1381/001
L-lysine hydrochloride, L-arginine hydrochloride
Novartis Europharm Limited
—
Maxitrol 0.1% w/v, 6000 IU/ml, 3500 IU/ml eye drops, suspension PA0896/019/001
Dexamethasone, Polymyxin b sulfate, Neomycin sulfate
Novartis Ireland Limited
Not marketed
Mayzent 0.25 mg film-coated tablets EU/1/19/1414/001-002
Siponomid, SIPONIMOD FUMARIC ACID
Novartis Europharm Limited
—
Mayzent 1 mg film-coated tablets EU/1/19/1414/007-008
SIPONIMOD FUMARIC ACID
Novartis Europharm Limited
—
Mayzent 2 mg film-coated tablets EU/1/19/1414/003
Siponomid, SIPONIMOD FUMARIC ACID
Novartis Europharm Limited
—
Myfortic 180 mg gastro-resistant tablets PA0896/023/001
Mycophenolic acid
Novartis Ireland Limited
Marketed
Myfortic 360 mg gastro-resistant tablets PA0896/023/002
Mycophenolic acid
Novartis Ireland Limited
Marketed
Neoral 100mg Soft Capsules PA0896/024/003
Ciclosporin
Novartis Ireland Limited
Marketed
Neoral 25 mg Soft Capsules PA0896/024/001
Ciclosporin
Novartis Ireland Limited
Marketed
Neoral 50mg Soft Capsules PA0896/024/002
Ciclosporin
Novartis Ireland Limited
Marketed
Neparvis 24 mg/26 mg film-coated tablets EU/1/16/1103/001
Sacubitril valsartan
Novartis Europharm Limited
—
Neparvis 49 mg/51 mg film-coated tablets EU/1/16/1103/002-004
Sacubitril valsartan
Novartis Europharm Limited
—
Neparvis 97 mg/103 mg film-coated tablets EU/1/16/1103/005-007
Sacubitril valsartan
Novartis Europharm Limited
—
Opatanol EU/1/02/217/002
Olopatadine hydrochloride
Novartis Europharm Limited
—
Opatanol 1 mg/mL eye drops, solution EU/1/02/217/001
Olopatadine hydrochloride
Novartis Europharm Limited
—
Showing 101–150 of 223
Cite this view

Priya Life Science (2026). Irish Medicines Register, filtered. Derived from the HPRA open dataset. Retrieved 29 September 2026. https://priyalifescience.com/medicines

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