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PRODUCT DETAIL

Kerendia 20 mg filmom obalené tablety

Code 9845D
MA number EU/1/21/1616/007
Product Form: tbl flm 28x20 mg (blis.PVC/PVDC/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Bayer AG, Germany
Therapeutic Class: 50 - DIURETICA
ATC:
C CARDIOVASCULAR SYSTEM
C03 DIURETICS
C03D POTASSIUM-SPARING AGENTS
C03DA Aldosterone antagonists
C03DA05 Finerenone
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: 16.02.2022
Validity: 16.02.2027
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 11.03.2022
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