Sweden· SE-20240628000141
ROMVIMZA 30 mg Kapsel, hård
A medicinal product containing vimseltinib, registered in Sweden by Deciphera Pharmaceuticals (Netherlands) B.V..
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Vimseltinib
- Manufacturer
- Deciphera Pharmaceuticals (Netherlands) B.V.
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer20240628000141
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Vimseltinib in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesROMVIMZADeciphera Pharmaceuticals, LLC
- CzechiaROMVIMZADeciphera Pharmaceuticals (Netherlands) B.V., Amsterdam
- SpainROMVIMZA 30 MG CAPSULAS DURASDeciphera Pharmaceuticals (Netherlands) B.V.
- FinlandROMVIMZADeciphera Pharmaceuticals (Netherlands) B.V.
- FranceROMVIMZA 30 mg, géluleDECIPHERA PHARMACEUTICALS (NETHERLANDS) (PAYS-BAS)
- BelgiumRomvimza 30 mgDeciphera Pharmaceuticals (Netherlands)
- IcelandROMVIMZADeciphera Pharmaceuticals (Netherlands) B.V.
- NetherlandsROMVIMZA 30 mg harde capsulesDeciphera Pharmaceuticals (Netherlands) B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Romvimza
- Liechtenstein · Romvimza
- Norway · Romvimza
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Swedish Medical Products Agency (Sweden). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/aba52c38-cebb-4cd1-96f8-1093ff38c44f GET /v1/drugs/aba52c38-cebb-4cd1-96f8-1093ff38c44f?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"source": "lakemedelsverket",
"doc_types": [
"EPAR",
"EMA"
],
"se_npl_id": "20240628000141",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20240628000141",
"product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/romvimza-epar-product-information_sv.pdf"
}See everything about vimseltinib.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.