The marketing authorisation for Nespo has been withdrawn at the request of the marketing authorisation holder.
Nespo : EPAR - Summary for the public (PDF/276.77 KB)
First published: 29/01/2009
Last updated: 29/01/2009
|Agency product number||
|International non-proprietary name (INN) or common name||
|Therapeutic area (MeSH)||
|Anatomical therapeutic chemical (ATC) code||
Dompé Biotec S.p.A.
|Date of issue of marketing authorisation valid throughout the European Union||
28/10/2008 Nespo - EMEA/H/C/000333 - II/0047
- Annex I - Summary of product characteristics
- Annex IIA - Manufacturing-authorisation holder responsible for batch release
- Annex IIB - Conditions of the marketing authorisation
- Annex IIIA - Labelling
- Annex IIIB - Package leaflet
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Treatment of symptomatic anaemia associated with chronic renal failure (CRF) in adults and paediatric patients.
Treatment of symptomatic anaemia in adult cancer patients with non-myeloid malignancies receiving chemotherapy.