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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
Tybost 150 mg film-coated tablets
EU/1/13/872/001-002
Cobicistat on silicon dioxide Gilead Sciences Ireland UC
Tyedra 1500 micrograms tablet
PA25435/001/001
Levonorgestrel micronized Maxmind Pharmaceutical GmbH Not marketed
Tyenne 162 mg solution for injection in pre-filled pen
EU/1/23/1754/010-012
Tocilizumab Fresenius Kabi Deutschland GmbH
Tyenne 162 mg solution for injection in pre-filled syringe
EU/1/23/1754/007-009
Tocilizumab Fresenius Kabi Deutschland GmbH
Tyenne 20 mg/mL concentrate for solution for infusion
EU/1/23/1754/001-006
Tocilizumab Fresenius Kabi Deutschland GmbH
Tygacil 50 mg powder for solution for infusion
EU/1/06/336/01
Tigecycline Pfizer Europe MA EEIG
Tyruko 300 mg concentrate for solution for infusion
EU/1/23/1745/001
Natalizumab Polpharma Biologics S.A.
Tysabri 150 mg solution for injection in pre-filled syringe
EU/1/06/346/002
Natalizumab Biogen Netherlands B.V.
Tysabri 300 mg concentrate for solution for infusion
EU/1/06/346/001
Natalizumab Biogen Netherlands B.V.
Tyvense 20 mg capsules, hard
PA23211/005/001
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyvense 30 mg capsules, hard
PA23211/005/002
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyvense 40 mg capsules, hard
PA23211/005/003
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyvense 50 mg capsules, hard
PA23211/005/004
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyvense 60 mg capsules, hard
PA23211/005/005
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyvense 70 mg capsules, hard
PA23211/005/006
Lisdexamfetamine dimesylate Takeda Pharmaceuticals International AG Ireland Branch Marketed
Tyverb 250 mg film-coated tablets
EU/1/07/440/1-2
Lapatinib ditosylate monohydrate Novartis Europharm Limited
Ucedane 200 mg dispersible tablets
EU/1/17/1202/001-002
Carglumic acid Eurocept International BV
Ultibro Breezhaler 85 micrograms/43 micrograms inhalation powder hard capsules
EU/1/13/862/001-006
Indacaterol maleate, Glycopyrronium bromide Novartis Europharm Limited
Ultomiris 1 100 mg/11 mL concentrate for solution for infusion
EU/1/19/1371/003
RAVULIZUMAB Alexion Europe S.A.S.
Ultomiris 300 mg/3 mL concentrate for solution for infusion
EU/1/19/1371/002
RAVULIZUMAB Alexion Europe S.A.S.
Ulunar Breezhaler 85 micrograms/43 micrograms inhalation powder hard capsules
EU/1/14/917/001-006
Indacaterol maleate, Glycopyrronium bromide Novartis Europharm Limited
UNIPHYLLIN 200 mg Prolonged-Release Tablets
PA23369/003/001
Theophylline Ennogen Healthcare (Europe) Limited Not marketed
UNIPHYLLIN 300 mg Prolonged-Release Tablets
PA23369/003/002
Theophylline Ennogen Healthcare (Europe) Limited Not marketed
UNIPHYLLIN 400 mg Prolonged-Release Tablets
PA23369/003/003
Theophylline Ennogen Healthcare (Europe) Limited Not marketed
Uplizna 100 mg concentrate for solution for infusion
EU/1/21/1602/001
Inebilizumab Amgen Europe B.V.,
Upstaza 2.8 × 10^11 vector genomes/0.5 mL solution for infusion
EU/1/22/1653/001
Eladocagene Exuparvovec PTC Therapeutics International Limited
Uptravi 100 microgram film-coated tablets
EU/1/15/1083/012-013
Selexipag Janssen-Cilag International NV
Uptravi 1000 microgram film-coated tablets
EU/1/15/1083/007
Selexipag Janssen-Cilag International NV
Uptravi 1200 microgram film-coated tablets
EU/1/15/1083/008
Selexipag Janssen-Cilag International NV
Uptravi 1400 microgram film-coated tablets
EU/1/15/1083/009
Selexipag Janssen-Cilag International NV
Uptravi 1600 microgram film-coated tablets
EU/1/15/1083/010
Selexipag Janssen-Cilag International NV
Uptravi 200 microgram film-coated tablets
EU/1/15/1083/001-003
Selexipag Janssen-Cilag International NV
Uptravi 400 microgram film-coated tablets
EU/1/15/1083/004
Selexipag Janssen-Cilag International NV
Uptravi 600 microgram film-coated tablets
EU/1/15/1083/005
Selexipag Janssen-Cilag International NV
Uptravi 800 microgram film-coated tablets
EU/1/15/1083/006
Selexipag Janssen-Cilag International NV
Urorec 4 mg hard capsules
EU/1/09/608/1-7
Silodosin Recordati Ireland Limited
Urorec 8 mg hard capsules
EU/1/09/608/8-14
Silodosin Recordati Ireland Limited
Usgena 130 mg concentrate for solution for infusion
EU/1/25/1987/005
Ustekinumab Stada Arzneimittel AG
Usgena 45 mg solution for injection
EU/1/25/1987/001
Ustekinumab Stada Arzneimittel AG
Usgena 45 mg solution for injection in pre-filled syringe
EU/1/25/1987/002
Ustekinumab Stada Arzneimittel AG
Usgena 90 mg solution for injection in pre-filled syringe
EU/1/25/1987/003-004
Ustekinumab Stada Arzneimittel AG
Usrenty 130 mg concentrate for solution for infusion
EU/1/25/1973/004
Ustekinumab Biocon Biologics Ireland Limited
Usrenty 45 mg solution for injection
EU/1/25/1973/001
Ustekinumab Biocon Biologics Ireland Limited
Usrenty 45 mg solution for injection in pre-filled syringe
EU/1/25/1973/002
Ustekinumab Biocon Biologics Ireland Limited
Usrenty 90 mg solution for injection in pre-filled syringe
EU/1/25/1973/003
Ustekinumab Biocon Biologics Ireland Limited
Usymro 130 mg concentrate for solution for infusion
EU/1/25/1957/004
Ustekinumab Gedeon Richter Plc
Usymro 45 mg solution for injection
EU/1/25/1957/001
Ustekinumab Gedeon Richter Plc
Usymro 45 mg solution for injection in pre-filled syringe
EU/1/25/1957/002
Ustekinumab Gedeon Richter Plc
Usymro 90 mg solution for injection in pre-filled syringe
EU/1/25/1957/003
Ustekinumab Gedeon Richter Plc
Uzpruvo 130 mg concentrate for solution for infusion
EU/1/23/1784/005
Ustekinumab Stada Arzneimittel AG
82 83 84 85 86 87 88
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.