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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

Pomalidomide Viatris 3 mg hard capsules EU/1/23/1785/009-012

Pomalidomide

Viatris Limited

—

Pomalidomide Viatris 4 mg hard capsules EU/1/23/1785/013-016

Pomalidomide

Viatris Limited

—

Posaconazole Viatris 100 mg gastro-resistant tablets PA23266/030/001

Posaconazole

Viatris Limited

Marketed

Prasugrel Viatris 10 mg EU/1/18/1273/002

Prasugrel

Mylan Pharmaceuticals Limited

—

Prasugrel Viatris 5 mg EU/1/18/1273/001

Prasugrel

Mylan Pharmaceuticals Limited

—

Pravastatin Viatris 10 mg Tablets PA23266/026/001

Pravastatin sodium

Viatris Limited

Not marketed

Pravastatin Viatris 20 mg Tablets PA23266/026/002

Pravastatin sodium

Viatris Limited

Not marketed

Pravastatin Viatris 40 mg Tablets PA23266/026/003

Pravastatin sodium

Viatris Limited

Not marketed

Pregabalin Mylan 100 mg hard capsules EU/1/15/997/023-027

Pregabalin

Viatris Limited

—

Pregabalin Mylan 150 mg hard capsules EU/1/15/997/028-034

Pregabalin

Viatris Limited

—

Pregabalin Mylan 200 mg hard capsules EU/1/15/997/035-039

Pregabalin

Viatris Limited

—

Pregabalin Mylan 225 mg hard capsules EU/1/15/997/040-044

Pregabalin

Viatris Limited

—

Pregabalin Mylan 25 mg hard capsules EU/1/15/997/001-008

Pregabalin

Viatris Limited

—

Pregabalin Mylan 300 mg hard capsules EU/1/15/997/045-050

Pregabalin

Viatris Limited

—

Pregabalin Mylan 50 mg hard capsules EU/1/15/997/009-015

Pregabalin

Viatris Limited

—

Pregabalin Mylan 75 mg hard capsules EU/1/15/997/016-022

Pregabalin

Viatris Limited

—

Pregabalin Viatris Pharma 100 mg hard capsules EU/1/14/916/020-023

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 150 mg hard capsules EU/1/14/916/024-029

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 200 mg hard capsules EU/1/14/916/030-033

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 225 mg hard capsules EU/1/14/916/034-037

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 25 mg hard capsules EU/1/14/916/001-007

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 300 mg hard capsules EU/1/14/916/038-043

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 50 mg hard capsules EU/1/14/916/008-013

Pregabalin

Viatris Healthcare Limited

—

Pregabalin Viatris Pharma 75 mg hard capsules EU/1/14/916/014-019

Pregabalin

Viatris Healthcare Limited

—

Rasagiline Mylan 1 mg tablets EU/1/16/1090/001-012

Rasagiline

Viatris Limited

—

Razolager 15 mg hard gastro-resistant capsules PA23266/074/001

Lansoprazole

Viatris Limited

Not marketed

Razolager 30 mg hard gastro-resistant capsules PA23266/074/002

Lansoprazole

Viatris Limited

Not marketed

Regurin 20 mg coated tablets PA23355/005/001

Trospium chloride

Viatris Healthcare Limited

Marketed

Relifex 1g film-coated tablets PA23355/039/002

Nabumetone

Viatris Healthcare Limited

Marketed

Relifex 500 mg film-coated Tablets PA23355/039/001

Nabumetone

Viatris Healthcare Limited

Marketed

RELPAX 40 mg film-coated tablets PA23355/049/001

ELETRIPTAN

Viatris Healthcare Limited

Marketed

Ritonavir Viatris 100 mg Film-coated tablet EU/1/17/1242/001-003

Ritonavir

Viatris Limited

—

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

—

Rosuvastatin 10 mg film-coated tablets PA23266/073/002

Rosuvastatin

Viatris Limited

Not marketed

Rosuvastatin 20 mg film-coated tablets PA23266/073/003

Rosuvastatin

Viatris Limited

Not marketed

Rosuvastatin 40 mg film-coated tablets PA23266/073/004

Rosuvastatin

Viatris Limited

Not marketed

Rosuvastatin 5 mg film-coated tablets PA23266/073/001

Rosuvastatin

Viatris Limited

Not marketed

Rosuvastatin Viatris 10 mg film-coated tablets PA23266/003/002

Rosuvastatin

Viatris Limited

Marketed

Rosuvastatin Viatris 20 mg film-coated tablets PA23266/003/003

Rosuvastatin

Viatris Limited

Marketed

Rosuvastatin Viatris 40 mg film-coated tablets PA23266/003/004

Rosuvastatin

Viatris Limited

Marketed

Rosuvastatin Viatris 5 mg film-coated tablets PA23266/003/001

Rosuvastatin

Viatris Limited

Marketed

Serc 16mg Tablets PA23355/014/002

Betahistine dihydrochloride

Viatris Healthcare Limited

Marketed

Serc 8mg Tablets PA23355/014/001

Betahistine dihydrochloride

Viatris Healthcare Limited

Marketed

Sevelamer Carbonate 800 mg film coated tablets PA23266/044/001

Sevelamer carbonate

Viatris Limited

Marketed

Simvastatin 10 mg Film-coated Tablets PA23266/047/001

Simvastatin

Viatris Limited

Marketed

Simvastatin 20 mg Film-coated Tablets PA23266/047/002

Simvastatin

Viatris Limited

Marketed

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

Download this register

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