The HPRA advises healthcare professionals not to retain printed versions of Summary of Product Characteristics (SPC) documents. As these documents are subject to frequent content updates, including changes to safety and dose related information, we recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about specific SPCs on our website then please e-mail info@hpra.ie


Temozolomide Sandoz



Sandoz GmbHEU/1/10/617/009-010

Main Information

Trade NameTemozolomide Sandoz
Active SubstancesTemozolomide
Dosage FormCapsule, hard
Licence HolderSandoz GmbH
Licence NumberEU/1/10/617/009-010

Group Information

ATC CodeL01AX Other alkylating agents
L01AX03 temozolomide

Status

License statusWithdrawn
Withdrawn Date15/09/2022
Legal statusProduct subject to prescription which may not be renewed (A)
Supply StatusSupply through pharmacies only
Advertising StatusAdvertising to healthcare professionals only
Conditions of LicenceMedicinal product subject to restricted medical prescription (See Annex I: Summary of Product Characteristics, section 4.2)
Marketing StatusUnknown

Documents

Summary of Product CharacteristicsSearch EMA website
Package LeafletSearch EMA website
Public Assessment ReportSearch EMA website

Generics Information

Interchangeable ListTemozolomide 100mg Capsules
Interchangeable List CodeIC0080-024-001
Interchangeable List DocumentPDF of Interchangeable List
« Back