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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
541 medicines starting with “R”
MedicineActive substanceLicence holderStatus
Rhophylac 300 micrograms/2 ml, solution for injection in pre-filled syringe
PA0800/006/002
Human anti-D immunoglobulin CSL Behring GmbH Marketed
Rhus tox
HOR1149/025/001
Rhus toxicodendron A. Nelson & Company Limited Not marketed
Riastap 1 g Powder for Solution for Injection/Infusion
PA0800/007/001
Human fibrinogen CSL Behring GmbH Not marketed
Ridate Once a Week 35mg film-coated tablets
PA0711/189/001
Risedronate sodium Rowex Limited, Marketed
Ridonex 10 mg orodispersible tablets
PA0126/291/001
Domperidone Clonmel Healthcare Ltd Marketed
Rifadin 100 mg/5 ml Oral Suspension
PA0540/066/004
Rifampicin Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifadin 150mg Capsules
PA0540/066/001
Rifampicin Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifadin 300mg Capsules
PA0540/066/002
Rifampicin Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifadin Intravenous 600mg Powder and Solvent for Concentrate for Solution for Infusion
PA0540/066/003
Rifampicin Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifater 50 mg/300 mg/120 mg Tablets
PA0540/067/001
Isoniazid, Pyrazinamide, Rifampicin Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifaximin Alfasigma 550 mg film-coated tablets
PA2206/001/001
Rifaximin Alfasigma S.p.A Not marketed
Rifinah 150/100 mg Film- Coated Tablets
PA0540/068/001
Rifampicin, Isoniazid Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Rifinah 300/150 mg Film Coated Tablets
PA0540/068/002
Rifampicin, Isoniazid Sanofi-Aventis Ireland Limited T/A SANOFI Marketed
Riltrava Aerosphere 5/7.2/160 micrograms pressurised inhalation, suspension
EU/1/21/1604/001-002
Formoterol fumarate dihydrate, Glycopyrronium bromide, Budesonide AstraZeneca AB
RILUTEK 50 mg film-coated tablets
EU/1/96/010/001
Riluzole Sanofi Winthrop Industrie
Riluzole Zentiva 50 mg film-coated tablets
EU/1/12/768/001
Riluzole Aventis Pharma S.A.
Rimmyrah
EU/1/23/1779/001-002
Ranibizumab Qilu Pharma Spain S.L.
Ringer’s Solution for Infusion, Viaflo container
PA2299/011/001
Sodium chloride, Potassium chloride, Calcium chloride dihydrate Baxter Holding B.V. Marketed
Rinozal 5 mg film-coated tablets
PA0126/179/001
Levocetirizine dihydrochloride Clonmel Healthcare Ltd Marketed
RINVOQ 15 mg prolonged-release tablets
EU/1/19/1404/001-005
UPADACITINIB, Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
RINVOQ 30 mg prolonged-release tablets
EU/1/19/1404/006-009
Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
RINVOQ 45 mg prolonged-release tablets
EU/1/19/1404/010-011
Upadacitinib Hemihydrate AbbVie Deutschland GmbH & Co. KG
Risedronate Bluefish Once a Week 35 mg film-coated tablets
PA1436/017/001
Risedronate sodium hemipentahydrate Bluefish Pharmaceuticals AB Marketed
Risedronate Sodium Accord Once a Week 35 mg film-coated tablets
PPA0465/165/001
Risedronate sodium PCO Manufacturing Ltd.
Risonate Once Weekly 35 mg Film-coated Tablets
PA0749/064/001
Risedronate sodium Teva Pharma B.V. Marketed
Risontel Once a week 35mg film-coated tablets
PA0126/197/001
Risedronate sodium Clonmel Healthcare Ltd Marketed
RISPERDAL 0.5 mg film-coated tablets
PA22612/010/009
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL 1 mg film-coated tablets
PA22612/010/004
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL 1 mg/ml oral solution
PA22612/010/001
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL 1 mg/ml oral solution
PPA2306/007/001
Risperidone Originalis B.V.
RISPERDAL 1 mg/ml oral solution
PPA1463/227/001
Risperidone IMED Healthcare Ltd.,
RISPERDAL 1 mg/ml oral solution
PPA0465/525/001
Risperidone PCO Manufacturing Ltd.
RISPERDAL 2 mg film-coated tablets
PA22612/010/005
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL 3 mg film-coated tablets
PA22612/010/006
Risperidone Janssen Sciences Ireland Unlimited Company Not marketed
RISPERDAL 4 mg film-coated tablets
PA22612/010/007
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL 6 mg film-coated tablets
PA22612/010/002
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL CONSTA 25 mg powder and solvent for prolonged-release suspension for injection
PA22612/010/010
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL CONSTA 37.5 mg powder and solvent for prolonged-release suspension for injection
PA22612/010/011
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
RISPERDAL CONSTA 50 mg powder and solvent for prolonged-release suspension for injection
PA22612/010/012
Risperidone Janssen Sciences Ireland Unlimited Company Marketed
Risperidone 1 mg/ml oral solution
PA0281/248/001
Risperidone Pinewood Laboratories Ltd Not marketed
Risperidone Grindeks 0.5 mg film-coated tablets
PA22992/021/001
Risperidone AS Grindeks Not marketed
Risperidone Grindeks 1 mg film-coated tablets
PA22992/021/002
Risperidone AS Grindeks Not marketed
Risperidone Grindeks 2 mg film-coated tablets
PA22992/021/003
Risperidone AS Grindeks Not marketed
Risperidone Grindeks 3 mg film-coated tablets
PA22992/021/004
Risperidone AS Grindeks Not marketed
Risperidone Grindeks 4 mg film-coated tablets
PA22992/021/005
Risperidone AS Grindeks Not marketed
Risperidone Grindeks 6 mg film-coated tablets
PA22992/021/006
Risperidone AS Grindeks Not marketed
Rispeva 0.5 mg film-coated tablets
PA1986/021/001
Risperidone Teva B.V. Marketed
Rispeva 1 mg film-coated tablets
PA0749/049/007
Risperidone Teva Pharma B.V. Marketed
Rispeva 2 mg film-coated tablets
PA0749/049/008
Risperidone Teva Pharma B.V. Marketed
Rispeva 3 mg film-coated tablets
PA0749/049/009
Risperidone Teva Pharma B.V. Marketed
3 4 5 6 7 8 9
Cite this database

Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 6 July 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.