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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
Atomoxetine Azure 100 mg hard capsules
PA22871/034/007
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atomoxetine Azure 18 mg hard capsules
PA22871/034/002
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atomoxetine Azure 25 mg hard capsules
PA22871/034/003
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atomoxetine Azure 40 mg hard capsules
PA22871/034/004
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atomoxetine Azure 60 mg hard capsules
PA22871/034/005
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atomoxetine Azure 80 mg hard capsules
PA22871/034/006
Atomoxetine hydrochloride Azure Pharmaceuticals Ltd. Not marketed
Atorvastatin 10mg film-coated tablets
PA2050/003/001
Atorvastatin Sun Pharmaceutical Industries Europe B.V. Marketed
Atorvastatin 20 mg film-coated tablets
PA2050/003/002
Atorvastatin Sun Pharmaceutical Industries Europe B.V. Marketed
Atorvastatin 40 mg film-coated tablets
PA2050/003/003
Atorvastatin Sun Pharmaceutical Industries Europe B.V. Marketed
Atorvastatin 80 mg film-coated tablets
PA2050/003/004
Atorvastatin Sun Pharmaceutical Industries Europe B.V. Marketed
Atorvastatin Bluefish 10 mg Film-coated tablets
PA1436/027/001
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Bluefish 20 mg Film-coated tablets
PA1436/027/002
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Bluefish 30 mg Film-coated tablets
PA1436/027/003
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Bluefish 40 mg Film-coated tablets
PA1436/027/004
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Bluefish 60 mg Film-coated tablets
PA1436/027/005
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Bluefish 80 mg Film-coated tablets
PA1436/027/006
Atorvastatin calcium trihydrate Bluefish Pharmaceuticals AB Marketed
Atorvastatin Rowa 10 mg film-coated tablets
PA0074/079/001
Atorvastatin Rowa Pharmaceuticals Limited, Marketed
Atorvastatin Rowa 20 mg film-coated tablets
PA0074/079/002
Atorvastatin Rowa Pharmaceuticals Limited, Marketed
Atorvastatin Rowa 40 mg film-coated tablets
PA0074/079/003
Atorvastatin Rowa Pharmaceuticals Limited, Marketed
Atorvastatin Rowa 80 mg film-coated tablets
PA0074/079/004
Atorvastatin Rowa Pharmaceuticals Limited, Marketed
Atosiban SUN 37.5 mg/5 ml concentrate for solution for infusion
EU/1/13/852/002
Atosiban Sun Phamaceutical Industries Europe B.V.
Atosiban SUN 6.75 mg/0.9 ml solution for injection
EU/1/13/852/001
Atosiban Sun Phamaceutical Industries Europe B.V.
ATRIANCE 5mg/ml Solution for Infusion
EU/1/07/403/001
Nelarabine Sandoz Pharmaceuticals d.d.
Attrogy 250 mg film-coated tablets
EU/1/25/1929/001
Diflunisal AO Pharma AB
AUBAGIO 14 mg film-coated tablets
EU/1/13/838/001-005
Teriflunomide Sanofi Winthrop Industrie
AUBAGIO 7 mg film-coated tablets
EU/1/13/838/006
Teriflunomide Sanofi Winthrop Industrie
Aucatzyl 410 × 106 cells dispersion for infusion
EU/1/25/1951/001
Obecabtagene autoleucel Autolus GmbH
AUGTYRO 160 mg hard capsules
EU/1/24/1883/003-004
Repotrectinib Bristol-Myers Squibb Pharma EEIG
AUGTYRO 40 mg hard capsules
EU/1/24/1883/001-002
Repotrectinib Bristol-Myers Squibb Pharma EEIG
AVAMYS 27.5 micrograms/spray, nasal spray suspension
EU/1/07/434/001-003
Fluticasone furoate GlaxoSmithKline Trading Services Limited
Avastin 25 mg/ml concentrate for solution for infusion
EU/1/04/300/001-002
Bevacizumab Roche Registration GmbH
Avastin 25 mg/ml Concentrate for solution for infusion
EU/1/04/300/1-2
Bevacizumab Roche Registration Limited
AVONEX 30 micrograms/0.5 ml solution for injection.
EU/1/97/033/003
Interferon beta - 1a Biogen Netherlands B.V.
Avtozma 162 mg solution for injection in pre-filled pen
EU/1/24/1896/010-012
Tocilizumab Celltrion Healthcare Hungary Kft.
Avtozma 162 mg solution for injection in pre-filled syringe
EU/1/24/1896/007-009
Tocilizumab Celltrion Healthcare Hungary Kft.
Avtozma 20 mg/mL concentrate for solution for infusion
EU/1/24/1896/001-006
Tocilizumab Celltrion Healthcare Hungary Kft.
Avzivi 25 mg/mL concentrate for solution for infusion
EU/1/24/1834/001-002
Bevacizumab Biosimilar FGK Representative Service GmbH
Awiqli 700 units/mL solution for injection in pre-filled pen
EU/1/24/1815/001-014
Insulin icodec Novo Nordisk A/S
Axitinib Accord 1 mg Film-coated tablet
EU/1/24/1847/001-005
Axitinib Accord Healthcare S.L.U.
Axitinib Accord 3 mg Film-coated tablet
EU/1/24/1847/006-010
Axitinib Accord Healthcare S.L.U.
Axitinib Accord 5 mg Film-coated tablet
EU/1/24/1847/011-015
Axitinib Accord Healthcare S.L.U.
Axsain 0.075% w/w Cream
PA23369/004/001
Capsaicin Ennogen Healthcare (Europe) Limited Marketed
Axumin 1,600 MBq/mL solution for injection
EU/1/17/1186/001
Fluciclovine (18f) Blue Earth Diagnostics Ireland Ltd
Axumin 3,200 MBq/mL solution for injection
EU/1/17/1186/002
Fluciclovine (18f) Blue Earth Diagnostics Ireland Ltd
Axura 10 mg film-coated tablets
EU/1/02/218/1-3
Memantine hydrochloride Merz Pharmaceuticals GmbH
Axura 20 mg film-coated tablets
EU/1/02/218/17-22
Memantine Merz Pharmaceuticals GmbH
Axura 5 mg+10 mg+15 mg+20 mg film-coated tablets
EU/1/02/218/16
Memantine Merz Pharmaceuticals GmbH
Axura 5 mg/pump actuation oral solution
EU/1/02/218/5-6
Memantine hydrochloride Merz Pharmaceuticals GmbH
Aybintio 25 mg/ml concentrate for solution for infusion
EU/1/20/1454/001
Bevacizumab Samsung Bioepis NL B.V.
Aybintio 25 mg/ml concentrate for solution for infusion
EU/1/20/1454/002
Bevacizumab Samsung Bioepis NL B.V.
5 6 7 8 9 10 11
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 15 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.