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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

Trulicity 4.5 mg Solution for injection EU/1/14/956/014-0016

Dulaglutide

Eli Lilly Nederland B.V.

—

Valerian Complex Stress Relief Oral Drops TR2309/020/001

A.Vogel Ireland Limited

Marketed

Vaxelis suspension for injection in pre-filled syringe. Diphtheria, tetanus, pertussis (acellular, component), hepatitis B (rDNA), poliomyelitis (inactivated), and Haemophilus type b conjugate vaccine (adsorbed). EU/1/15/1079/001-007

Diphtheria toxoid adsorbed, Tetanus toxoid adsorbed

MCM Vaccine B.V.

—

Verzenios 100 mg Film-coated tablet EU/1/18/1307/004-006

ABEMACICLIB

Eli Lilly Nederland B.V.

—

Verzenios 150 mg Film-coated tablet EU/1/18/1307/007-009

ABEMACICLIB

Eli Lilly Nederland B.V.

—

Verzenios 50 mg Film-coated tablet EU/1/18/1307/001-003

ABEMACICLIB

Eli Lilly Nederland B.V.

—

Voltarol Muscle & Joint Pain Relief 140 mg medicated plaster PA0678/140/004

Diclofenac sodium

Haleon Ireland Limited

Not marketed

WELIREG 40 mg film-coated tablets EU/1/24/1893/001-002

Belzutifan

Merck Sharp & Dohme BV,

—

Xagrid 0.5 mg hard capsules EU/1/04/295/001

Anagrelide hydrochloride

Takeda Pharmaceuticals International AG Ireland Branch

—

Xylocaine 10 mg/delivered dose Mucosal Spray PA1691/028/001

Lidocaine

Aspen Pharma Trading Limited

Marketed

Yentreve EU/1/04/280/1-6

Duloxetine hydrochloride

Eli Lilly Nederland B.V.

—

Yentreve 20 mg hard gastro-resistant capsules EU/1/04/280/001

Duloxetine hydrochloride

Eli Lilly Nederland B.V.

—

Yondelis 0.25 mg Powder for concentrate for solution for infusion EU/1/07/417/1

Trabectedin

Pharma Mar S.A.

—

Yondelis 1 mg Powder for concentrate for solution for infusion EU/1/07/417/2

Trabectedin

Pharma Mar S.A.

—

Zeliravel 400 microgram hard modified-release capsules PA23266/070/001

Tamsulosin hydrochloride

Viatris Limited

Not marketed

Zirtek Allergy Relief 10 mg film-coated tablets PA0891/008/005

Cetirizine dihydrochloride

UCB (Pharma) Ireland Limited,

Marketed

Zoladex 3.6 mg implant PA1019/027/001

Goserelin

Marketed

Zoladex 3.6 mg implant PPA1463/125/001

Goserelin

IMED Healthcare Ltd.,

—

Zoladex LA 10.8 mg implant PA1019/027/002

Goserelin

Marketed

Zoladex LA 10.8 mg implant PPA1463/125/002

Goserelin

IMED Healthcare Ltd.,

—

Zoladex LA 10.8 mg Implant PPA2306/027/001

Goserelin

Originalis B.V.

—

Zydelig 100 mg film-coated tablets EU/1/14/938/001

Idelalisib

Gilead Sciences Ireland UC

—

Zydelig 150 mg film-coated tablets EU/1/14/938/002

Idelalisib

Gilead Sciences Ireland UC

—

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

GET /api/export.php?register=medicines-ie&format=csv Try the JSON export →

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