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PRODUCT DETAIL

BEYONTTRA 356 mg filmom obalené tablety

Code 8993E
MA number EU/1/24/1906/001
Product Form: tbl flm 120x356 mg (blis. PVC/PCTFE/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: BridgeBio Europe B.V., Netherland
Therapeutic Class: 41 - CARDIACA
ATC:
C CARDIOVASCULAR SYSTEM
C01 CARDIAC THERAPY
C01E OTHER CARDIAC PREPARATIONS
C01EB Other cardiac preparations
C01EB25 Acoramidis
Shelf life: 30
Container: blister PVC/PCTFE/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 10.02.2025
Validity: 10.02.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 13.02.2025
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