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PRODUCT DETAIL

Ocrevus 920 mg injekčný roztok

Code 7041E
MA number EU/1/17/1231/003
Product Form: sol inj 1x23 ml/920 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Roche Registration GmbH, Germany
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AG ?
L04AG08 Ocrelizumab
Shelf life: 24
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 08.01.2018
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 08.08.2024
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