S.I. No. 625/2025 - Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2025 Skip to content Disclaimer Feedback Helpdesk Gaeilge Léim go dtí an t-ábhar Séanadh Aiseolas Deasc chabhrach English Gaeilge English Produced by the Office of the Attorney General Táirgthe ag Oifig an Ard-Aighne Home Legislation Acts of the Oireachtas Statutory Instruments Pre-1922 Legislation Constitution External Resources Bills (Houses of the Oireachtas) Iris Oifigiúil / Official Gazette Revised Acts (LRC) Classified List of Legislation (LRC) Translations (acts.
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- s)or rangeBliain nó blianta nó raon TypeCineál All Legislation Acts Statutory Instruments Advanced SearchCuardach Casta HomeBaile Statutory InstrumentsIonstraimí Reachtúla 2025 S.I. No. 625/2025 - Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2025 S.I. No. 625/2025 - Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2025 AmendmentsLeasuithe Download PDF Íoslódáil PDF Notice of the making of this Statutory Instrument was published in “Iris Oifigiúil” of 30th December, 2025. I, JENNIFER CARROLL MACNEILL, Minister for Health, in exercise of the powers conferred on me by section 32 (as amended by section 9 of the Health (Miscellaneous Provisions) Act 2024 (No. 23 of 2024)) of the Irish Medicines Board Act 1995 (No. 29 of 1995), hereby make the following regulations: 1. These Regulations may be cited as the Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2025. 2. The collective citation “the Medicinal Products (Prescription and Control of Supply) Regulations 2003 to 2025” includes these regulations. 3. In these Regulations “Principal Regulations” means the Medicinal Products (Prescription and Control of Supply) Regulations 2003 ( S.I. No. 540 of 2003 ). 4. The Thirteenth Schedule (as inserted by Regulation 8 of the Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2025 ( S.I. No. 502 of 2025 )) to the Principal Regulations is amended by inserting after the entry for “Trimethoprim” the following entry: “ Medicinal Product Strength Pharmaceutical Form Purpose Column 1 Column 2 Column 3 Column 4 Trimethoprim 200mg Tablets For the treatment of symptoms consistent with uncomplicated lower urinary tract infection (cystitis), in accordance with the relevant protocol approved by the Minister for Health ”. GIVEN under my Official Seal, 17 December, 2025. JENNIFER CARROLL MACNEILL, Minister for Health. EXPLANATORY NOTE (This note is not part of the Instrument and does not purport to be a legal interpretation.) These Regulations amend the Medicinal Products (Prescription and Control of Supply) Regulations 2003. The purpose of these Regulations is to update the schedule of medicinal products which may be prescribed by registered pharmacists pursuant to Regulation 5C of the Medicinal Products (Prescription and Control of Supply) Regulations 2003. These Regulations may be cited as the Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2025. Privacy Statement Accessibility European Legislation Identifier (PDF) Open Data License Ráiteas Príobháideachais Inrochtaineacht Aitheantóir Eorpach Reachtaíochta (ELI) Ceadúnas Sonraí Oscailte Liosta Fianán © Government of Ireland. Oireachtas Copyright Material is reproduced with the permission of the Houses of the Oireachtas © Rialtas na hÉireann. Atáirgtear ábhar faoi Chóipcheart le cead ó Thithe an Oireachtais