QUVIVIQ 50 mg filmom obalené tablety

Code 0665E
MA number EU/1/22/1638/004
Product Form: tbl flm 30x50 mg (blis. PVC/PVDC/PVC/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Shelf life: 36
Container: blister PVC/PVDC/PVC/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 29.04.2022
Validity: 29.04.2027
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 04.07.2023
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