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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
Stalpex 50 microgram/500 microgram/dose inhalation powder, pre-dispensed
PA22815/001/001
Salmeterol, Fluticasone propionate Glenmark Pharmaceuticals Nordic AB
STAMICIS 1mg kit for radiopharmaceutical preparation
PA0677/018/001
Tetrakis (2-methoxy isobutyl isonitrile) copper (i) tetrafluorolborate CIS bio International Marketed
STAYVEER 125 mg film-coated tablets
EU/1/13/832/002
Bosentan monohydrate Janssen Pharmaceutica NV
STAYVEER 62.5 mg film-coated tablets
EU/1/13/832/001
Bosentan monohydrate Janssen Pharmaceutica NV
Steglatro 15 mg film-coated tablets
EU/1/18/1267/007-012
Ertugliflozin l-pyroglutamic acid Merck Sharp & Dohme BV
Steglatro 5 mg film-coated tablets
EU/1/18/1267/001-006
Ertugliflozin l-pyroglutamic acid Merck Sharp & Dohme BV
Steglujan 15 mg/100 mg film-coated tablets
EU/1/18/1266/007-012
Ertugliflozin l-pyroglutamic acid, Sitagliptin phosphate monohydrate Merck Sharp & Dohme BV
Steglujan 5 mg/100 mg film-coated tablets
EU/1/18/1266/001-006
Ertugliflozin l-pyroglutamic acid, Sitagliptin phosphate monohydrate Merck Sharp & Dohme BV
STELARA 130 mg Concentrate for solution for infusion
EU/1/08/494/005
Ustekinumab Janssen-Cilag International NV
STELARA 45 mg Solution for injection
EU/1/08/494/003
Ustekinumab Janssen-Cilag International NV
STELARA 45 mg Solution for injection
EU/1/08/494/001
Ustekinumab Janssen-Cilag International NV
STELARA 90 mg Solution for injection
EU/1/08/494/004
Ustekinumab Janssen-Cilag International NV
STEQEYMA 130 mg Concentrate for solution for infusion
EU/1/24/1844/003
Ustekinumab Celltrion Healthcare Hungary Kft.
STEQEYMA 45 mg Solution for injection
EU/1/24/1844/001
Ustekinumab Celltrion Healthcare Hungary Kft.
STEQEYMA 90 mg Solution for injection
EU/1/24/1844/002
Ustekinumab Celltrion Healthcare Hungary Kft.
Sterile Dopamine Concentrate BP 160mg/ml, 5ml
PA0073/108/002
DOPAMINE HYDROCHLORIDE Mercury Pharmaceuticals (Ireland) Ltd Not marketed
Sterile Dopamine Concentrate BP 40mg/ml
PA0073/108/001
DOPAMINE HYDROCHLORIDE Mercury Pharmaceuticals (Ireland) Ltd Not marketed
Stimufend 6 mg solution for injection in pre-filled syringe
EU/1/22/1632/001
Pegfilgrastim Fresenius Kabi Deutschland GmbH
Stivarga 40 mg film-coated tablets
EU/1/13/858/001-002
Regorafenib Bayer Pharma AG
Stoboclo 60 mg solution for injection in pre-filled syringe
EU/1/24/1905/001
Denosumab Celltrion Healthcare Hungary Kft.
Stocrin
EU/1/99/111/003
Efavirenz Merck Sharp & Dohme BV,
Stocrin
EU/1/99/111/004
Efavirenz Merck Sharp & Dohme BV,
STOCRIN
EU/1/99/111/001
Efavirenz Merck Sharp & Dohme BV,
STOCRIN
EU/1/99/111/002
Efavirenz Merck Sharp & Dohme BV,
STOCRIN 200 mg film-coated tablets
EU/1/99/111/011
Efavirenz Merck Sharp & Dohme BV,
STOCRIN 30 mg/mL oral solution
EU/1/99/111/005
Efavirenz Merck Sharp & Dohme BV,
STOCRIN 50 mg film-coated tablets
EU/1/99/111/010
Efavirenz Merck Sharp & Dohme BV,
Stocrin Film-Coated
EU/1/99/111/6-7
Efavirenz Merck Sharp & Dohme BV,
Stocrin Film-Coated
EU/1/99/111/8-9
Efavirenz Merck Sharp & Dohme BV,
Strensiq 100 mg/ml solution for injection
EU/1/15/1015/003-004
Asfotase alfa Alexion Europe SAS
Strensiq 40 mg/ml solution for injection
EU/1/15/1015/001-002
Asfotase alfa Alexion Europe SAS
Strepsils Intensive Honey & Eucalyptus Sugar Free 8.75 mg lozenges
PA0979/080/001
Flurbiprofen Reckitt Benckiser Ireland Limited
Striascan 74 MBq /mL solution for injection
EU/1/19/1372/001-002
IOFLUPANE (1231) CIS bio International
Stribild 150 mg/150 mg/200 mg/245 mg film-coated tablets
EU/1/13/830/001
Emtricitabine, Tenofovir disoproxil, Cobicistat, Elvitegravir Gilead Sciences Ireland UC
Strimvelis 1-10 x 10e6 cells/mL dispersion for infusion
EU/1/16/1097/001
Autologous cd34+ enriched cell fraction Fondazione Telethon Ets
Suboxone 12 mg/3 mg Sublingual film
EU/1/06/359/016-018
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate Indivior Europe Limited
Suboxone 16 mg/4 mg Sublingual tablet
EU/1/06/359/005-006
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate Indivior Europe Limited
Suboxone 2 mg/0.5 mg Sublingual film
EU/1/06/359/007-009
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate Indivior Europe Limited
Suboxone 2 mg/0.5 mg Sublingual tablet
EU/1/06/359/01-02
Naloxone, Buprenorphine Indivior Europe Limited
Suboxone 4 mg/1 mg Sublingual film
EU/1/06/359/010-012
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate Indivior Europe Limited
Suboxone 8 mg/2 mg Sublingual film
EU/1/06/359/013-015
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate Indivior Europe Limited
Suboxone 8 mg/2 mg Sublingual tablet
EU/1/06/359/03-04
Buprenorphine hydrochloride, NALOXONE HYDROCHLORIDE Indivior Europe Limited
Sugammadex 100 mg/mL solution for injection
PA23250/012/001
Sugammadex sodium MSN Labs Europe Limited Not marketed
Sugammadex Adroiq 100 mg/mL solution for injection
EU/1/23/1733/001-002
Sugammadex sodium Extrovis EU Kft.
Sugammadex Fresenius Kabi 100 mg/mL solution for injection
EU/1/22/1663/001-003
Sugammadex Fresenius Kabi Deutschland GmbH
Sugammadex Mylan 100 mg/mL solution for injection
EU/1/21/1583/001-004
Sugammadex sodium Mylan Pharmaceuticals Limited
Sugammadex Piramal 100 mg/mL solution for injection
EU/1/23/1739/001-002
Sugammadex sodium Piramal Critical Care B.V.
Sugammadex – Amomed®
EU/1/22/1708/001
Sugammadex sodium Aop Orphan Pharmaceuticals GmbH
Suliqua 100 units/ml + 33 micrograms/ml solution for injection in pre-filled pen
EU/1/16/1157/003-004
Lixisenatide, Insulin glargine Sanofi-Aventis Groupe
Suliqua 100 units/ml + 50 micrograms/ml solution for injection in pre-filled pen
EU/1/16/1157/001-002
Insulin glargine, Lixisenatide Sanofi-Aventis Groupe
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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.