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PRODUCT DETAIL

Tecentriq 1 875 mg injekčný roztok

Code 5339E
MA number EU/1/17/1220/003
Product Form: sol inj 1x15 ml/1875 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Roche Registration GmbH, Germany
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01F MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES
L01FF PD-1/PDL-1 (Programmed cell death protein 1/death ligand 1) inhibitors
L01FF05 Atezolizumab
Shelf life: 24
Container: glass vial
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 21.09.2017
SmPC + PL: European Medicines Agency's database
Dokument: Tecentriq_Karta pacienta.pdf  
Safety feature Yes
Data update: 02.02.2024
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