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Irish Medicines Database · HPRA register

Neupogen Singleject 48 MU/0.5 ml Solution for injection in a pre-filled syringe filgrastim

Authorisation PA1026/001/008 · Amgen Europe B.V.,

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Neupogen Singleject 48 MU/0.5 ml Solution for injection in a pre-filled syringe filgrastim
Licence PA1026/001/008 · Marketed
Licence holder
Amgen Europe B.V., (all products →)
Active substance
Filgrastim
Dosage form
Solution for injection in pre-filled syringe
Routes of administration
Intravenous use, Subcutaneous use
ATC codes
L03AA, L03AA02
First authorised
16/11/2001
Prescription status
Product subject to prescription which may not be renewed (A)
Supply
Supply through pharmacies only
Legal basis
Full application (Article 8(3) of Directive No 2001/83/EC)

Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 04 Jul 2026. This listing is regulatory information, not medical advice — consult the package leaflet, SPC, or a healthcare professional. For the authoritative record see the HPRA register.