Pharmaceuticals - Community Register


Community list of not active medicinal products for human use


Product information

Invented name: Topotecan Eagle
Auth. number : EU/1/11/744
Active substance : topotecan
ATC: Anatomical main group: L - Antineoplastic and immunomodulating agents
Therapeutic subgroup: L01 - Antineoplastic agents
Pharmacological subgroup: L01X - Other antineoplastic agents
Chemical subgroup: L01XX - Other antineoplastic agents
Chemical substance: L01XX17 - topotecan
(See WHO ATC Index)
Indication: Topotecan monotherapy is indicated for the treatment of patients with relapsed small cell lung cancer (SCLC) for whom re-treatment with the first-line regimen is not considered appropriate.
Topotecan in combination with cisplatin is indicated for patients with carcinoma of the cervix recurrent after radiotherapy and for patients with Stage IVB disease. Patients with prior exposure to cisplatin require a sustained treatment free interval to justify treatment with the combination.
Marketing Authorisation Holder: Eagle Laboratories Limited
The Clock House, Station Approach, Marlow, Bucks SL7 1NT, United Kingdom
EPAR and active package presentations

Package presentations

Information about presentations can be found in the website of the European Medicines Agency under the section "Product Information".
Likewise, presentations on which there has been a Commission decision are referred in the Summary of Product Characteristics (Annex I to the Commission Decision granting the marketing authorisation) which is available in the Community Register.

European Commission proceduresGoto top of the page

Close date procedure Procedure type EMEA number Decision summary publ decision docs annex
29/12/2011 Centralised - Authorisation - Decision addressed to Member States EMEA/H/C/2261 (2011)10098 of 22/12/2011
29/12/2011 Centralised - Authorisation EMEA/H/C/2261 (2011)10097 of 22/12/2011
13/03/2012 Centralised - Variation EMEA/H/C/2261/IB/1
Updated with Decision(2012)7103 of 04/10/2012
08/10/2012 Centralised - Variation (2012)7103 of 04/10/2012
03/10/2014 Centralised - Withdrawal (2014)7185 of 01/10/2014