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Medicines register · Ireland

Every medicine authorised for the Irish market

The Health Products Regulatory Authority's full list of authorised products — brand, active substance, licence holder, licence number and market status. Filter it, cite it, and take it away as a file.

Source: HPRA open dataset ("Authorised or Transfer Pending Products"), CC BY 4.0. Complete coverage — all 10,336 authorised products are in this register. Synced 20 Sep 2026, 17:51 UTC

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Matches brand name, active substance, licence holder and licence number.

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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

Medicine

Active substance

Licence holder

Status

Aclasta 5 mg solution for infusion EU/1/05/308/001

Zoledronic acid

Sandoz Pharmaceuticals d.d.

—

Afqlir EU/1/24/1867/001

Aflibercept

—

Afqlir EU/1/24/1867/002

Aflibercept

—

Aripiprazole Sandoz 10 mg Tablets EU/1/15/1029/015-028

Aripiprazole

—

Aripiprazole Sandoz 15 mg Tablets EU/1/15/1029/029-042

Aripiprazole

—

Aripiprazole Sandoz 20 mg Tablets EU/1/15/1029/043-047

Aripiprazole

—

Aripiprazole Sandoz 30 mg Tablets EU/1/15/1029/048-061

Aripiprazole

—

Aripiprazole Sandoz 5 mg Tablets EU/1/15/1029/001-014

Aripiprazole

—

ATRIANCE 5mg/ml Solution for Infusion EU/1/07/403/001

Nelarabine

Sandoz Pharmaceuticals d.d.

—

Binocrit 1 000 IU/0.5 mL solution for injection in a pre-filled syringe EU/1/07/410/1-2

Recombinant human erythropoietin alfa

—

Binocrit 10 000 IU/1 mL solution for injection in a pre-filled syringe EU/1/07/410/15-16

Recombinant human erythropoietin alfa

—

Binocrit 2 000 IU/1 mL solution for injection in a pre-filled syringe EU/1/07/410/3-4

Recombinant human erythropoietin alfa

—

Binocrit 20 000 IU/0.5 mL solution for injection in a pre-filled syringe EU/1/07/410/21-22

Epoetin alfa

—

Binocrit 3 000 IU/0.3 mL solution for injection in a pre-filled syringe EU/1/07/410/5-6

Recombinant human erythropoietin alfa

—

Binocrit 30 000 IU/0.75 mL solution for injection in a pre-filled syringe EU/1/07/410/23-24

Epoetin alfa

—

Binocrit 4 000 IU/0.4 mL solution for injection in a pre-filled syringe EU/1/07/410/7-8

Recombinant human erythropoietin alfa

—

Binocrit 40 000 IU/1 mL solution for injection in a pre-filled syringe EU/1/07/410/25-26

Epoetin alfa

—

Binocrit 5 000 IU/0.5 mL solution for injection in a pre-filled syringe EU/1/07/410/9-10

Recombinant human erythropoietin alfa

—

Binocrit 6 000 IU/0.6 mL solution for injection in a pre-filled syringe EU/1/07/410/11-12

Recombinant human erythropoietin alfa

—

Binocrit 8 000 IU/0.8 mL solution for injection in a pre-filled syringe EU/1/07/410/13-014

Recombinant human erythropoietin alfa

—

Brinzolamide Sandoz 10mg/ml eye drops, suspension PA0711/226/001

Brinzolamide

Marketed

Erelzi 25 mg solution for injection in pre-filled syringe EU/1/17/1195/001-004

Etanercept

—

Erelzi 50 mg solution for injection in pre-filled pen EU/1/17/1195/009-012

Etanercept

—

Erelzi 50 mg solution for injection in pre-filled syringe EU/1/17/1195/005-008

Etanercept

—

Estradot 100 micrograms/24 hours, transdermal patch PA23311/004/004

Estradiol

Sandoz Pharmaceuticals d.d.

Marketed

Estradot 25 micrograms/24 hours, transdermal patch PA23311/004/005

Estradiol

Sandoz Pharmaceuticals d.d.

Not marketed

Estradot 37.5 micrograms/24 hours, transdermal patch PA23311/004/001

Estradiol

Sandoz Pharmaceuticals d.d.

Marketed

Estradot 50 micrograms/24 hours, transdermal patch PA23311/004/002

Estradiol

Sandoz Pharmaceuticals d.d.

Marketed

Estradot 75 micrograms/24 hours, transdermal patch PA23311/004/003

Estradiol

Sandoz Pharmaceuticals d.d.

Marketed

Fortum 1 g powder for solution for injection or infusion PA23311/001/002

Ceftazidime

Sandoz Pharmaceuticals d.d.

Marketed

Fortum 2 g powder for solution for injection or infusion PA23311/001/003

Ceftazidime

Sandoz Pharmaceuticals d.d.

Marketed

Fortum 500 mg powder for solution for injection PA23311/001/001

Ceftazidime

Sandoz Pharmaceuticals d.d.

Marketed

Hefiya 20 mg solution for injection in pre-filled syringe EU/1/18/1287/007

Adalimumab

—

Hefiya 40 mg solution for injection in pre-filled pen EU/1/18/1287/004-006

Adalimumab

—

Hefiya 40 mg solution for injection in pre-filled syringe EU/1/18/1287/001-003

Adalimumab

—

Hefiya 80 mg solution for injection in pre-filled pen EU/1/18/1287/010-011

Adalimumab

—

Hefiya 80 mg solution for injection in pre-filled syringe EU/1/18/1287/008-009

Adalimumab

—

Herwenda 150 mg powder for concentrate for solution for infusion EU/1/23/1762/001

Trastuzumab

—

HYCAMTIN 0.25 mg hard capsules EU/1/96/027/006

Topotecan hydrochloride

Sandoz Pharmaceuticals d.d.

—

HYCAMTIN 1 mg hard capsules EU/1/96/027/007

Topotecan hydrochloride

Sandoz Pharmaceuticals d.d.

—

Hycamtin 1 mg powder for concentrate for solution for infusion EU/1/96/027/004

Topotecan (as hydrochloride)

Sandoz Pharmaceuticals d.d.

—

HYCAMTIN 1 mg powder for concentrate for solution for infusion EU/1/96/027/005

Topotecan (as hydrochloride)

Sandoz Pharmaceuticals d.d.

Marketed

Hycamtin 4 mg powder for concentrate for solution for infusion EU/1/96/027/003

Topotecan hydrochloride

Sandoz Pharmaceuticals d.d.

—

HYCAMTIN 4 mg powder for concentrate for solution for infusion EU/1/96/027/001

Topotecan hydrochloride

Sandoz Pharmaceuticals d.d.

—

Hyrimoz 20 mg solution for injection in pre-filled syringe EU/1/18/1286/007

Adalimumab

—

Hyrimoz 40 mg solution for injection in pre-filled pen EU/1/18/1286/004-006

Adalimumab

—

Hyrimoz 40 mg solution for injection in pre-filled syringe EU/1/18/1286/001-003

Adalimumab

—

Hyrimoz 80 mg solution for injection in pre-filled pen EU/1/18/1286/010-011

Adalimumab

—

Hyrimoz 80 mg solution for injection in pre-filled syringe EU/1/18/1286/008-009

Adalimumab

—

Ibandronic Acid Sandoz 50 mg film-coated tablets EU/1/11/685/001-005

Ibandronic acid

—

Cite this view

Priya Life Science (2026). Irish Medicines Register, filtered. Derived from the HPRA open dataset. Retrieved 28 September 2026. https://priyalifescience.com/medicines

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Regulatory information only — not medical advice. For the authoritative record see the HPRA register directly.