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PRODUCT DETAIL

Blenrep 70 mg prášok na koncentrát na infúzny roztok

Code 0834F
MA number EU/1/25/1948/001
Product Form: plc ifc 1x70 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: GlaxoSmithKline Trading Services Limited, Ireland
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01F MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES
L01FX Other monoclonal antibodies and antibody drug conjugates
L01FX15 Belantamab mafodotin
Shelf life: 48
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10a well-established use application
MA issued: 23.07.2025
Validity: 23.07.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 06.08.2025
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