Skip to Content


Active Substance: epoetin delta
Common Name: epoetin delta
ATC Code: B03XA
Marketing Authorisation Holder: Shire Pharmaceutical Contracts Limited
Active Substance: epoetin delta
Status: Withdrawn
Authorisation Date: 2002-03-18
Therapeutic Area: Anemia Kidney Failure, Chronic
Pharmacotherapeutic Group: Antianemic preparations

Therapeutic Indication

Dynepo is indicated for the treatment of symptomatic anaemia associated with chronic renal failure (CRF) in adult patients. It may be used in patients on dialysis and in patients not on dialysis.

The marketing authorisation for Dynepo has been withdrawn at the request of the marketing authorisation holder.

Source: European Medicines Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.