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Cerubidin 20 mg Powder for Concentrate for Solution for Infusion
Licence PA0540/096/001 · Marketed
- Licence holder
- Sanofi-Aventis Ireland Limited T/A SANOFI (all products →)
- Active substance
- Daunorubicin
- Dosage form
- Powder for concentrate for solution for infusion
- Route of administration
- Intravenous use
- ATC codes
- L01DB, L01DB02
- First authorised
- 20/04/1995
- Prescription status
- Product subject to prescription which may not be renewed (A)
- Supply
- Supply through pharmacies only
- Legal basis
- Full application (Article 8(3) 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.