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PRODUCT DETAIL

Itovebi 9 mg filmom obalené tablety

Code 0986F
MA number EU/1/25/1942/002
Product Form: tbl flm 28x1x9 mg (blis.Al/Al - jednotk.bal.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Roche Registration GmbH, Germany
Shelf life: 24
Container: blister Al/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: 18.07.2025
Validity: 18.07.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 02.09.2025
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