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

Filgrastim HEXAL

Hexal AGEU/1/08/496/1-4

Main Information

Trade NameFilgrastim HEXAL
Active SubstancesEp2006 (recombinant human granulocyte-colony stimulating factor)
Dosage FormSolution for injection in pre-filled syringe
Licence HolderHexal AG
Licence NumberEU/1/08/496/1-4

Group Information

ATC CodeL03AA Colony stimulating factors
L03AA02 filgrastim


License statusAuthorised
Licence Issued
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


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