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Updated 04 Jul 2026 · HPRA open data

Irish Medicines Database

Every medicine authorised for the Irish market — 10,165 products with active substances, licence holders, dosage forms and prescription status.

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
4,720 results for “eu”
MedicineActive substanceLicence holderStatus
Orladeyo 150 mg hard capsules
EU/1/21/1544/001
Berotralstat hydrochloride, Berotralstat BioCryst Ireland Ltd
Orphacol 250 mg hard capsules
EU/1/13/870/004-006
Cholic acid Theravia
Orphacol 50 mg hard capsules
EU/1/13/870/001-003
Cholic acid Theravia
ORSERDU 345 mg film-coated tablets
EU/1/23/1757/002
Elacestrant Dihydrochloride Stemline Therapeutics B.V.
ORSERDU 86 mg film-coated tablets
EU/1/23/1757/001
Elacestrant Dihydrochloride Stemline Therapeutics B.V.
Osenvelt 120 mg solution for injection
EU/1/24/1904/001-003
Denosumab Celltrion Healthcare Hungary Kft.
Oslif Breezhaler 150 microgram inhalation powder, hard capsules
EU/1/09/586/1-5
Indacaterol maleate Novartis Europharm Limited
Oslif Breezhaler 300 microgram inhalation powder, hard capsules
EU/1/09/586/6-10
Indacaterol maleate Novartis Europharm Limited
Osmohale, inhalation powder, hard capsule
PA22655/001/001
Mannitol Pharmaxis Europe Limited Marketed
Osvyrti 60mg Solution for injection in pre-filled syringe
EU/1/25/1922/002
Denosumab Accord Healthcare S.L.U.
Otezla 10 mg film-coated tablets Otezla 20 mg film-coated tablets
EU/1/14/981/004
Apremilast, Apremilast Amgen Europe B.V.,
Otezla 10 mg film-coated tablets Otezla 20 mg film-coated tablets Otezla 30 mg film-coated tablets
EU/1/14/981/001
Apremilast, Apremilast, Apremilast Amgen Europe B.V.,
Otezla 20 mg film–coated tablets
EU/1/14/981/005
Apremilast Amgen Europe B.V.,
Otezla 30 mg film-coated tablets
EU/1/14/981/002-003
Apremilast Amgen Europe B.V.,
Otulfi 130 mg Concentrate for solution for infusion
EU/1/24/1863/003
Ustekinumab Fresenius Kabi Deutschland GmbH
Otulfi 45 mg Solution for injection
EU/1/24/1863/001
Ustekinumab Fresenius Kabi Deutschland GmbH
Otulfi 45 mg Solution for injection pre-filled pen
EU/1/24/1863/005
Ustekinumab Fresenius Kabi Deutschland GmbH
Otulfi 90 mg Solution for injection
EU/1/24/1863/002
Ustekinumab Fresenius Kabi Deutschland GmbH
Otulfi 90 mg Solution for injection in Pre-filled pen
EU/1/24/1863/006
Ustekinumab Fresenius Kabi Deutschland GmbH
Ovaleap 300 IU/0.5 mL solution for injection
EU/1/13/871/001-003
Follitropin alfa Theramex Ireland Limited
Ovitrelle 250 micrograms solution for injection in pre-filled pen
EU/1/00/165/008
Choriogonadotropin alfa Merck Europe B.V.
Ovitrelle 250 micrograms/0.5 mL solution for injection in pre-filled syringe
EU/1/00/165/007
Choriogonadotropin alfa Ares-Serono (Europe) Limited
Oxaliplatin 5 mg/ml concentrate for solution for infusion
PA2059/049/001
Oxaliplatin Fresenius Kabi Deutschland GmbH Marketed
Oxbryta
EU/1/21/1622/001
Voxelotor Pfizer Europe MA EEIG
OXERVATE 20 micrograms/ml eye drops, solution
EU/1/17/1197/01
Recombinant human nerve growth factor (rhngf) Dompe farmaceutici SpA
Oxlumo 94.5 mg/0.5 mL solution for injection
EU/1/20/1496/001
Lumasiran sodium Alnylam Netherlands B.V.
OxyContin 10 mg prolonged release tablets
PA1688/005/002
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyContin 20 mg prolonged release tablets
PA1688/005/003
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyContin 40 mg prolonged release tablets
PA1688/005/004
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyContin 5 mg prolonged release tablets
PA1688/005/001
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyContin 80 mg prolonged release tablets
PA1688/005/005
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Not marketed
OxyNorm 10 mg hard capsules
PA1688/006/005
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm 10 mg/ml, solution for injection or infusion
PA1688/006/001
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm 20 mg hard capsules
PA1688/006/006
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm 5 mg hard capsules
PA1688/006/004
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm 50 mg/ml, solution for injection or infusion
PA1688/006/010
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm concentrate 10 mg/ml oral solution
PA1688/006/003
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm Dispersa 10 mg Orodispersible Tablets
PA1688/006/008
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm Dispersa 20 mg orodispersible tablets
PA1688/006/009
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm Dispersa 5 mg Orodispersible Tablets
PA1688/006/007
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
OxyNorm liquid 1 mg/ml oral solution
PA1688/006/002
OXYCODONE HYDROCHLORIDE Mundipharma Pharmaceuticals Limited Marketed
Oyavas 25 mg/mL concentrate for solution for infusion
EU/1/20/1510/001-002
Bevacizumab Stada Arzneimittel AG
Ozawade 18 mg film-coated tablets
EU/1/21/1546/002-003
Pitolisant hydrochloride Bioprojet Pharma
Ozawade 4.5 mg film-coated tablets
EU/1/21/1546/001
Pitolisant hydrochloride Bioprojet Pharma
Ozempic 0.25 mg solution for injection in pre-filled pen
EU/1/17/1251/002
Semaglutide Novo Nordisk A/S
Ozempic 0.5 mg solution for injection in pre-filled pen
EU/1/17/1251/003-004
Semaglutide Novo Nordisk A/S
Ozempic 0.5 mg solution for injection in pre-filled pen
EU/1/17/1251/012-013
Semaglutide Novo Nordisk A/S
Ozempic 1 mg solution for injection in pre-filled pen
EU/1/17/1251/005-006
Semaglutide Novo Nordisk A/S
Ozempic 2 mg solution for injection in pre-filled pen
EU/1/17/1251/010-011
Semaglutide Novo Nordisk A/S
OZURDEX 700 micrograms intravitreal implant in applicator
EU/1/10/638/001
Dexamethasone AbbVie Deutschland GmbH & Co. KG
55 56 57 58 59 60 61
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 16 August 2026).

Data: Health Products Regulatory Authority (HPRA) open dataset (“Authorised or Transfer Pending Products”), licensed CC BY 4.0, refreshed daily. Regulatory information only — not medical advice.