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PRODUCT DETAIL

Lacosamide UCB 10 mg/ml infúzny roztok

Code 2475D
MA number EU/1/19/1383/001
Product Form: sol inf 1x20 ml/200 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 21 - ANTIEPILEPTICA, ANTICONVULSIVA
ATC:
N NERVOUS SYSTEM
N03 ANTIEPILEPTICS
N03A ANTIEPILEPTICS
N03AX Other antiepileptics
N03AX18 Lacosamide
Shelf life: 36
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10c informed consent application
MA issued: 26.08.2019
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 09.05.2024
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