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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
OPDIVO 10 mg/mL concentrate for solution for infusion
EU/1/15/1014/001-004
Nivolumab Bristol-Myers Squibb Pharma EEIG
OPDIVO 600 mg solution for injection
EU/1/15/1014/005
Nivolumab Bristol-Myers Squibb Pharma EEIG
Opdualag 240 mg/80 mg sterile concentrate
EU/1/22/1679/001
RELATLIMAB, Nivolumab Bristol-Myers Squibb Pharma EEIG
Opfolda 65 mg hard capsules
EU/1/23/1737/001-002
Miglustat Amicus Therapeutics Europe Limited
Oprymea 0.088 mg tablets
EU/1/08/469/1-5
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.18 mg tablets
EU/1/08/469/6-10
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.26 mg prolonged-release tablets
EU/1/08/469/026-029
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.35 mg tablets
EU/1/08/469/11-15
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.52 mg prolonged-release tablets
EU/1/08/469/030-033
Pramipexole KRKA, d.d., Novo mesto
Oprymea 0.7 mg tablets
EU/1/08/469/16-20
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.05 mg prolonged-release tablets
EU/1/08/469/034-037
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.1 mg tablets
EU/1/08/469/21-25
Pramipexole KRKA, d.d., Novo mesto
Oprymea 1.57 mg prolonged-release tablets
EU/1/08/469/038-041
Pramipexole KRKA, d.d., Novo mesto
Oprymea 2.1 mg prolonged-release tablets
EU/1/08/469/042-045
Pramipexole KRKA, d.d., Novo mesto
Oprymea 2.62 mg prolonged-release tablets
EU/1/08/469/046-049
Pramipexole dihydrochloride monohydrate KRKA, d.d., Novo mesto
Oprymea 3.15 mg prolonged-release tablets
EU/1/08/469/050-053
Pramipexole dihydrochloride monohydrate KRKA, d.d., Novo mesto
Opsaren 10 mg Film-coated Tablets
PA22865/018/001
Macitentan Renata Pharmaceuticals (Ireland) Limited Not marketed
Opsumit 10 mg film-coated tablets
EU/1/13/893/001-002
Macitentan Janssen Pharmaceutica NV
Opsumit 2.5 mg film-coated tablets
EU/1/13/893/004
Macitentan Janssen Pharmaceutica NV
OPTISON 0.19 mg/ml dispersion for injection
EU/1/98/065/001
Perflutren, Human albumin microspheres GE Healthcare AS
OPTISON 0.19 mg/ml dispersion for injection
EU/1/98/065/002
Perflutren, Human albumin microspheres GE Healthcare AS
Optruma 60 mg film coated tablets
EU/1/98/074/001
Raloxifene Eli Lilly Nederland B.V.
Optruma 60 mg film coated tablets
EU/1/98/074/002
Raloxifene Eli Lilly Nederland B.V.
Optruma 60 mg film coated tablets
EU/1/98/074/003
Raloxifene Eli Lilly Nederland B.V.
Optruma 60 mg film coated tablets
EU/1/98/074/004
Raloxifene Eli Lilly Nederland B.V.
Opuviz 40 mg/mL solution for injection in a vial
EU/1/24/1865/001-002
Aflibercept Samsung Bioepis NL B.V.
Opzelura 15 mg/g Cream
EU/1/23/1726/001
Ruxolitinib Incyte Biosciences Distribution B.V.
Oramox 125 mg/5 ml powder for oral suspension
PA1418/013/001
Amoxicillin Athlone Pharmaceuticals Limited Marketed
Oramox 250 mg hard capsules
PA1418/013/003
Amoxicillin Athlone Pharmaceuticals Limited Marketed
Oramox 250 mg/5 ml powder for oral suspension
PA1418/013/002
Amoxicillin Athlone Pharmaceuticals Limited Marketed
Oramox 500 mg hard capsules
PA1418/013/004
Amoxicillin Athlone Pharmaceuticals Limited Marketed
Ordspono 2 mg Concentrate for solution for infusion
EU/1/24/1843/001
Odronextamab Regeneron Ireland Designated Activity Company
Ordspono 320 mg Concentrate for solution for infusion
EU/1/24/1843/003
Odronextamab Regeneron Ireland Designated Activity Company
Ordspono 80 mg Concentrate for solution for infusion
EU/1/24/1843/002
Odronextamab Regeneron Ireland Designated Activity Company
Orencia 125 mg solution for injection in pre-filled pen
EU/1/07/389/004-009
Abatacept Bristol-Myers Squibb Pharma EEIG
Orencia 125 mg solution for injection in pre-filled pen
EU/1/07/389/011-012
Abatacept Bristol-Myers Squibb Pharma EEIG
Orencia 250 mg powder for concentrate for solution for infusion
EU/1/07/389/1-3
Abatacept Bristol-Myers Squibb Pharma EEIG
Orencia 50 mg solution for injection in pre-filled syringe
EU/1/07/389/013
Abatacept Bristol-Myers Squibb Pharma EEIG
Orencia 87.5 mg solution for injection in pre-filled syringe
EU/1/07/389/014
Abatacept Bristol-Myers Squibb Pharma EEIG
ORFADIN
EU/1/04/303/1-3
Nitisinone Swedish Orphan International AB
Orfadin 20 mg hard capsules
EU/1/04/303/004
Nitisinone Swedish Orphan Biovitrum AB
Orfadin 4 mg/ml oral suspension
EU/1/04/303/005
Nitisinone Swedish Orphan Biovitrum AB
Orgalutran 0.25 mg/0.5 mL solution for injection
EU/1/00/130/001
Ganirelix N.V. Organon
Orgalutran 0.25 mg/0.5 mL solution for injection
EU/1/00/130/002
Ganirelix N.V. Organon
Orgovyx 120 mg film-coated tablets
EU/1/22/1642/001
Relugolix Accord Healthcare S.L.U.
Orkambi 100 mg/125 mg film-coated tablets
EU/1/15/1059/005
Lumacaftor, Ivacaftor Vertex Pharmaceuticals (Ireland) Limited
Orkambi 100 mg/125 mg granules in sachet
EU/1/15/1059/006
Lumacaftor, Ivacaftor Vertex Pharmaceuticals (Ireland) Limited
Orkambi 150 mg/188 mg granules in sachet
EU/1/15/1059/007
Ivacaftor, Lumacaftor Vertex Pharmaceuticals (Ireland) Limited
Orkambi 200 mg/125 mg film-coated tablets
EU/1/15/1059/001
Lumacaftor, Ivacaftor Vertex Pharmaceuticals (Ireland) Limited
Orkambi 75 mg/94 mg granules in sachet
EU/1/15/1059/008
Lumacaftor, Ivacaftor Vertex Pharmaceuticals (Ireland) Limited
54 55 56 57 58 59 60
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.