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PRODUCT DETAIL

VYDURA 75 mg perorálny lyofilizát

Code 1441E
MA number EU/1/22/1645/003
Product Form: lyo por 16x1x75 mg (blis.PVC/OPA/Al) - jednotk.bal.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 33 - ANTIMIGRAENICA,ANTISEROTONICA
ATC:
N NERVOUS SYSTEM
N02 ANALGESICS
N02C ANTIMIGRAINE PREPARATIONS
N02CD Calcitonin gene-related peptide (CGRP) antagonists
N02CD06 Rimegepant
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 25.04.2022
Validity: 25.04.2027
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 28.06.2022
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