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Oramox 125 mg/5 ml powder for oral suspension
Licence PA1418/013/001 · Marketed
- Licence holder
- Athlone Pharmaceuticals Limited (all products →)
- Active substance
- Amoxicillin
- Dosage form
- Powder for oral suspension
- Route of administration
- Oral use
- ATC codes
- J01CA, J01CA04
- First authorised
- 27/09/1988
- Prescription status
- Product subject to prescription which may not be renewed (A)
- Supply
- Supply through pharmacies only
- Legal basis
- Informed consent application (Article 10c of Directive No 2001/83/EC)
Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 04 Jul 2026. This listing is regulatory information, not medical advice — consult the package leaflet, SPC, or a healthcare professional. For the authoritative record see the HPRA register.