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PRODUCT DETAIL

LEMTRADA 12 mg infúzny koncentrát

Code 7211A
MA number EU/1/13/869/001
Product Form: con inf 1x1,2 ml/12 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Sanofi Belgium, Belgium
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AA Selective immunosuppressants
L04AA34 Alemtuzumab
Shelf life: 48
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - known active substance
MA issued: 12.09.2013
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 14.07.2023
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