Fludara 50 mg powder for solution for injection or infusion
- Licence status
- Withdrawn: 03/01/2023
- Active substances
- Fludarabine phosphate
- Dosage Form
- Powder for solution for injection/infusion
- Licence number
- PA0611/004/001
- Licence holder
- Sanofi B.V.
Product documents
- Package Leaflet
- Summary of Product Characteristics
- Public Assessment Report
Licence information
- ATC code
- L01BB Purine analogues, L01BB05 fludarabine
- Legal supply status
- Product subject to prescription which may not be renewed (A)
- Place of sale
- Supply through pharmacies only
- Marketing availability
- Marketed
- Advertising conditions
- Advertising to healthcare professionals only
- Licence issued
- 12/12/1994