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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
ReFacto AF 1000 IU powder and solvent for solution for injection
EU/1/99/103/003
Recombinant antihemophilic factor Pfizer Europe MA EEIG
ReFacto AF 1000 IU powder and solvent for solution for injection in pre-filled syringe
EU/1/99/103/007
Moroctocog alfa Pfizer Europe MA EEIG
ReFacto AF 2000 IU powder and solvent for solution for injection
EU/1/99/103/004
Recombinant antihemophilic factor Pfizer Europe MA EEIG
ReFacto AF 2000 IU powder and solvent for solution for injection in pre-filled syringe
EU/1/99/103/008
Moroctocog alfa Pfizer Europe MA EEIG
ReFacto AF 250 IU powder and solvent for solution for injection
EU/1/99/103/001
Recombinant antihemophilic factor Pfizer Europe MA EEIG
ReFacto AF 3000 IU powder and solvent for solution for injection in pre-filled syringe
EU/1/99/103/005
Moroctocog alfa Pfizer Europe MA EEIG
ReFacto AF 500 IU powder and solvent for solution for injection
EU/1/99/103/002
Recombinant antihemophilic factor Pfizer Europe MA EEIG
ReFacto AF 500 IU powder and solvent for solution for injection in pre-filled syringe
EU/1/99/103/006
Moroctocog alfa Pfizer Europe MA EEIG
Refixia 1 000 IU powder and solvent for solution for injection
EU/1/17/1193/002
Nonacog beta pegol Novo Nordisk A/S
Refixia 2 000 IU powder and solvent for solution for injection
EU/1/17/1193/003
Nonacog beta pegol Novo Nordisk A/S
Refixia 3 000 IU powder and solvent for solution for injection
EU/1/17/1193/004
Nonacog beta pegol Novo Nordisk A/S
Refixia 500 IU powder and solvent for solution for injection
EU/1/17/1193/001
Nonacog beta pegol Novo Nordisk A/S
REKAMBYS 600 mg prolonged-release suspension for injection
EU/1/20/1482/001
Rilpivirine Janssen-Cilag International NV
REKAMBYS 900 mg prolonged-release suspension for injection
EU/1/20/1482/002
Rilpivirine Janssen-Cilag International NV
REKOVELLE 12 micrograms/0.36 mL solution for injection in a pre-filled pen
EU/1/16/1150/004
Follitropin delta Ferring Pharmaceuticals A/S
REKOVELLE 36 micrograms/1.08 mL solution for injection in a pre-filled pen
EU/1/16/1150/005
Follitropin delta Ferring Pharmaceuticals A/S
Rekovelle 72 micrograms/2.16 mL solution for injection in a pre-filled pen
EU/1/16/1150/006
Follitropin delta Ferring Pharmaceuticals A/S
Relistor
EU/1/08/463/004-008
Methylnaltrexone bromide Bausch Health Ireland Limited
Relistor
EU/1/08/463/8-11
Methylnaltrexone bromide Bausch Health Ireland Limited
RELISTOR 12 mg/0.6 mL solution for injection
EU/1/08/463/1-3
Methylnaltrexone bromide Bausch Health Ireland Limited
Relvar Ellipta 184 micrograms/22 micrograms inhalation powder, pre-dispensed
EU/1/13/886/004-006
Fluticasone furoate, Vilanterol trifenatate micronised GlaxoSmithKline (Ireland) Limited
Relvar Ellipta 92 micrograms/22 micrograms inhalation powder, pre-dispensed
EU/1/13/886/001-003
Fluticasone furoate, Vilanterol trifenatate micronised GlaxoSmithKline (Ireland) Limited
Remicade 100 mg Powder for concentrate for solution for infusion
EU/1/99/116/001-5
Infliximab Janssen-Cilag International NV
Remifentanil 1 mg powder for concentrate for solution for injection or infusion
PA2059/056/001
Remifentanil Fresenius Kabi Deutschland GmbH Not marketed
Remifentanil 2 mg powder for concentrate for solution for injection or infusion
PA2059/056/002
Remifentanil Fresenius Kabi Deutschland GmbH Not marketed
Remifentanil 5 mg powder for concentrate for solution for injection or infusion
PA2059/056/003
Remifentanil Fresenius Kabi Deutschland GmbH Not marketed
Remsima 100 mg powder for concentrate for solution for infusion
EU/1/13/853/001
Infliximab Celltrion Healthcare Hungary Kft.
Remsima 120 mg solution for injection in pre-filled pen
EU/1/13/853/012-014
Infliximab Celltrion Healthcare Hungary Kft.
Remsima 120 mg solution for injection in pre-filled syringe
EU/1/13/853/006-011
Infliximab Celltrion Healthcare Hungary Kft.
Remsima 40 mg/mL concentrate for solution for infusion
EU/1/13/853/018-027
Infliximab Celltrion Healthcare Hungary Kft.
Renagel
EU/1/99/123/006
Sevelamer Sanofi Winthrop Industrie
Renagel
EU/1/99/123/007
Sevelamer Sanofi Winthrop Industrie
Renagel
EU/1/99/123/009
Sevelamer Sanofi Winthrop Industrie
Renagel
EU/1/99/123/010
Sevelamer Sanofi Winthrop Industrie
Renagel
EU/1/99/123/011-013
Sevelamer Sanofi Winthrop Industrie
Renagel 400 mg Film-coated tablet
EU/1/99/123/005-007
Sevelamer Sanofi Winthrop Industrie
Renagel 800 mg Film-coated tablet
EU/1/99/123/008-013
Sevelamer Sanofi Winthrop Industrie
RENOCIS 1 mg kit for radiopharmaceutical preparation
PA0677/005/001
Succimer CIS bio International Marketed
Renvela 0.8 g Powder for oral suspension
EU/1/09/521/008-009
Sevelamer carbonate Sanofi Winthrop Industrie
Renvela 0.8 g Powder for oral suspension (with dosing spoon)
EU/1/09/521/009
Sevelamer carbonate Sanofi Winthrop Industrie
Renvela 1.6 g Powder for oral suspension
EU/1/09/521/4-5
Sevelamer carbonate Sanofi Winthrop Industrie
Renvela 2.4 g Powder for oral suspension
EU/1/09/521/6-7
Sevelamer carbonate Sanofi Winthrop Industrie
Renvela 800 mg Film-coated tablet
EU/1/09/521/1-3
Sevelamer carbonate Sanofi Winthrop Industrie
Repaglinide Accord 0.5 mg tablets
EU/1/11/743/001-005
Repaglinide Accord Healthcare S.L.U.
Repaglinide Accord 1 mg tablets
EU/1/11/743/006-010
Repaglinide Accord Healthcare S.L.U.
Repaglinide Accord 2 mg tablets
EU/1/11/743/011-015
Repaglinide Accord Healthcare S.L.U.
Repaglinide Krka 0.5 mg tablets
EU/1/09/579/1-6
Repaglinide KRKA, d.d., Novo mesto
Repaglinide Krka 1 mg tablets
EU/1/09/579/7-12
Repaglinide KRKA, d.d., Novo mesto
Repaglinide Krka 2 mg tablets
EU/1/09/579/13-18
Repaglinide KRKA, d.d., Novo mesto
Repaglinide Teva 0.5 mg Tablet
EU/1/09/530/1-5
Repaglinide Teva Pharma B.V.
65 66 67 68 69 70 71
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.