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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
Riluzole Zentiva 50 mg film-coated tablets
EU/1/12/768/001
Riluzole Aventis Pharma S.A.
Rimmyrah
EU/1/23/1779/001-002
Ranibizumab Qilu Pharma Spain S.L.
RINVOQ 15 mg prolonged-release tablets
EU/1/19/1404/001-005
UPADACITINIB, Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
RINVOQ 30 mg prolonged-release tablets
EU/1/19/1404/006-009
Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
RINVOQ 45 mg prolonged-release tablets
EU/1/19/1404/010-011
Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
Risedronate Bluefish Once a Week 35 mg film-coated tablets
PA1436/017/001
Risedronate sodium hemipentahydrate Bluefish Pharmaceuticals AB Marketed
Ristaben 100 mg film-coated tablets
EU/1/10/621/13-18
Sitagliptin as monohydrate phosphate salt Merck Sharp & Dohme BV,
Ristaben 25 mg film-coated tablets
EU/1/10/621/1-6
Sitagliptin as monohydrate phosphate salt Merck Sharp & Dohme BV
Ristaben 50 mg film-coated tablets
EU/1/10/621/7-12
Sitagliptin as monohydrate phosphate salt Merck Sharp & Dohme BV,
Ristfor 50 mg/1000 mg film-coated tablets
EU/1/10/620/009-016
Metformin Hydrochloride, Sitagliptin phosphate Merck Sharp & Dohme BV,
Ristfor 50 mg/850 mg film-coated tablets
EU/1/10/620/1-8
Metformin Hydrochloride, Sitagliptin phosphate Merck Sharp & Dohme BV
Ritonavir Viatris 100 mg Film-coated tablet
EU/1/17/1242/001-003
Ritonavir Viatris Limited
RIULVY 174 mg gastro-resistant hard capsules
EU/1/25/1947/001-002
Tegomil fumarate Neuraxpharm Pharmaceuticals S.L.
RIULVY 348 mg gastro-resistant hard capsules
EU/1/25/1947/003-005
Tegomil fumarate Neuraxpharm Pharmaceuticals S.L.
Rivaroxaban 10 mg film-coated tablets
PA22865/010/001
Rivaroxaban Renata Pharmaceuticals (Ireland) Limited Not marketed
Rivaroxaban 15 mg film-coated tablets
PA22865/010/002
Rivaroxaban Renata Pharmaceuticals (Ireland) Limited Not marketed
Rivaroxaban 20 mg film-coated tablets
PA22865/010/003
Rivaroxaban Renata Pharmaceuticals (Ireland) Limited Not marketed
Rivaroxaban Accord 10 mg film-coated tablets
EU/1/20/1488/012-023
Rivaroxaban Accord Healthcare S.L.U.
Rivaroxaban Accord 15 mg film-coated tablets
EU/1/20/1488/024-038
Rivaroxaban Accord Healthcare S.L.U.
Rivaroxaban Accord 15 mg film-coated tablets Rivaroxaban Accord 20 mg film-coated tablets
EU/1/20/1488/039
Rivaroxaban, Rivaroxaban Accord Healthcare S.L.U.
Rivaroxaban Accord 2.5 mg film-coated tablets
EU/1/20/1488/001-011
Rivaroxaban Accord Healthcare S.L.U.
Rivaroxaban Accord 20 mg film-coated tablets
EU/1/20/1488/040-053
Rivaroxaban Accord Healthcare S.L.U.
Rivaroxaban Azure 10 mg film-coated tablets
PA1963/019/002
Rivaroxaban Cipla Europe Not marketed
Rivaroxaban Azure 15 mg film-coated tablets
PA1963/019/003
Rivaroxaban Cipla Europe Not marketed
Rivaroxaban Azure 15 mg film-coated tablets Rivaroxaban Azure 20 mg film-coated tablets
PA1963/019/005
Rivaroxaban, Rivaroxaban Cipla Europe Not marketed
Rivaroxaban Azure 2.5 mg film-coated tablets
PA1963/019/001
Rivaroxaban Cipla Europe Not marketed
Rivaroxaban Azure 20 mg film-coated tablets
PA1963/019/004
Rivaroxaban Cipla Europe Not marketed
Rivaroxaban Bluefish 10 mg film-coated tablets
PA1436/044/001
Rivaroxaban Bluefish Pharmaceuticals AB Not marketed
Rivaroxaban Bluefish 15 mg film-coated tablets
PA1436/044/002
Rivaroxaban Bluefish Pharmaceuticals AB Not marketed
Rivaroxaban Bluefish 15 mg film-coated tablets Rivaroxaban Bluefish 20 mg film-coated tablets
PA1436/044/004
Rivaroxaban, Rivaroxaban Bluefish Pharmaceuticals AB Not marketed
Rivaroxaban Bluefish 20 mg film-coated tablets
PA1436/044/003
Rivaroxaban Bluefish Pharmaceuticals AB Not marketed
Rivaroxaban MSN 10 mg film-coated tablets
PA23250/004/002
Rivaroxaban MSN Labs Europe Limited Not marketed
Rivaroxaban MSN 15 mg film-coated tablets
PA23250/004/003
Rivaroxaban MSN Labs Europe Limited Not marketed
Rivaroxaban MSN 2.5 mg film-coated tablets
PA23250/004/001
Rivaroxaban MSN Labs Europe Limited Not marketed
Rivaroxaban MSN 20 mg film-coated tablets
PA23250/004/004
Rivaroxaban MSN Labs Europe Limited Not marketed
Rivaroxaban Rowa 10 mg film-coated tablets
PA0074/097/001
Rivaroxaban Rowa Pharmaceuticals Limited, Not marketed
Rivaroxaban Rowa 15 mg film-coated tablets
PA0074/097/002
Rivaroxaban Rowa Pharmaceuticals Limited, Not marketed
Rivaroxaban Rowa 20 mg film-coated tablets
PA0074/097/003
Rivaroxaban Rowa Pharmaceuticals Limited, Not marketed
Rivaroxaban Viatris 10 mg film-coated tablets
EU/1/21/1588/015-025
Rivaroxaban Viatris Limited
Rivaroxaban Viatris 15 mg film-coated tablets
EU/1/21/1588/026-040
Rivaroxaban Viatris Limited
Rivaroxaban Viatris 15 mg film-coated tablets Rivaroxaban Viatris 20 mg film-coated tablets
EU/1/21/1588/055
Rivaroxaban, Rivaroxaban Viatris Limited
Rivaroxaban Viatris 2.5 mg film-coated tablets
EU/1/21/1588/001-014
Rivaroxaban Viatris Limited
Rivaroxaban Viatris 20 mg film-coated tablets
EU/1/21/1588/041-054
Rivaroxaban Viatris Limited
Rivastigmine 1 A Pharma 1.5 mg hard capsules
EU/1/09/585/001-4
Rivastigmine hydrogen tartrate 1 A Pharma GmbH
Rivastigmine 1 A Pharma 2 mg/ml oral solution
EU/1/09/585/017-018
Rivastigmine hydrogen tartrate 1 A Pharma GmbH
Rivastigmine 1 A Pharma 3 mg hard capsules
EU/1/09/585/005-8
Rivastigmine hydrogen tartrate 1 A Pharma GmbH
Rivastigmine 1 A Pharma 4.5 mg hard capsules
EU/1/09/585/009-12
Rivastigmine hydrogen tartrate 1 A Pharma GmbH
Rivastigmine 1 A Pharma 6 mg hard capsules
EU/1/09/585/013-16
Rivastigmine hydrogen tartrate 1 A Pharma GmbH
Rivastigmine Actavis 1.5 mg hard capsules
EU/1/11/693/001-004
Rivastigmine hydrogen tartrate Actavis Group hf
Rivastigmine Actavis 3 mg hard capsules
EU/1/11/693/005-008
Rivastigmine hydrogen tartrate Actavis Group hf
67 68 69 70 71 72 73
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.