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PRODUCT DETAIL

Nintedanib Viatris 150 mg mäkké kapsuly

Code 1022F
MA number EU/1/25/1959/004
Product Form: cps mol 60x1x150 mg (blis.Al/Al - jednotk.bal.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Viatris Limited, Ireland
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01E Protein kinase inhibitors
L01EX Other protein kinase inhibitors
L01EX09 Nintedanib
Shelf life: 36
Container: blister Al/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 22.08.2025
Validity: 22.08.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 05.09.2025
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