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PRODUCT DETAIL

ROMVIMZA 30 mg tvrdé kapsuly

Code 1317F
MA number EU/1/25/1968/003
Product Form: cps dur 8x30 mg (blis.OPA/Al/PVC)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU Orphan
MAH, country: Deciphera Pharmaceuticals (Netherlands) B.V, Netherland
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01E Protein kinase inhibitors
L01EX Other protein kinase inhibitors
L01EX29 Vimseltinib
Shelf life: 36
Container: blister OPA/Al/PVC
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: 17.09.2025
Validity: 17.09.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 09.10.2025
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