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PRODUCT DETAIL

Vimpat 50 mg filmom obalené tablety

Code 5619D
MA number EU/1/08/470/032
Product Form: tbl flm 60x50 mg (fľ.HDPE)
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: 60
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 17.09.2008
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 06.10.2020
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