en

PRODUCT DETAIL

Neulasta 6 mg injekčný roztok

Code 41011
MA number EU/1/02/227/002
Product Form: sol inj 1x0,6 ml/6 mg (napln.skl.inj.striek.-neblistr.bal.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L03 Immunomodulators/-stimulants
L03A Immunostimulants
L03AA Colony stimulating factors
L03AA13 Pegfilgrastim
Shelf life: 36
Container: glass pre-filled syringe
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 22.08.2002
SmPC + PL: European Medicines Agency's database
Dokument: DHPC filgastrim 3 9 2013.pdf  
Safety feature Yes
Data update: 19.06.2018
eu-flag.png sk-flag.png