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Prednisolone 20 mg Rectal Foam
Licence PA22643/003/001 · Marketed
- Licence holder
- Chemidex Pharma Limited (all products →)
- Active substance
- Prednisolone sodium metasulfobenzoate
- Dosage form
- Rectal foam
- Route of administration
- Rectal use
- ATC codes
- D07AA, D07AA03
- First authorised
- 11/02/2011
- Prescription status
- Product subject to prescription which may not be renewed (A)
- Supply
- Supply through pharmacies only
- Legal basis
- Not Currently Available
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.