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PRODUCT DETAIL

Bortezomib SUN 3,5 mg prášok na injekčný roztok

Code 0826C
MA number EU/1/16/1102/001
Product Form: plv ino 1x3,5 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01X OTHER ANTINEOPLASTIC AGENTS
L01XG Proteasome inhibitors
L01XG01 Bortezomib
Shelf life: 36
Container: glass vial
Route of admin.: Subcutaneous and intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 22.07.2016
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 12.10.2022
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