Netherlands· NL-c1e6b66b100c
Aumseqa 55 mg filmomhulde tablet
A aumolertinib product containing aumolertinibmesilaat, registered in Netherlands by SFL Pharmaceuticals Deutschland GmbH. The same ATC class is registered in 8 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Aumolertinib is registered in 8 of 19 countries.
Countries holding a registration under ATC L01EB11 (aumolertinib), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 5 of them publish a price we can compare per daily dose
Aumolertinib · ATC L01EB11
8 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- AUMOLERTINIBMESILAAT
- Manufacturer
- SFL Pharmaceuticals Deutschland GmbH
- Country
- Netherlands (NL)
- ATC code
- L01EB11
- ATC class
- Aumolertinib
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/25/2006
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Aumolertinib in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumAumseqa 55 mgSfl Pharmaceuticals Deutschland
- CzechiaAUMSEQASFL Pharmaceuticals Deutschland GmbH, Lörrach
- FinlandAumseqaSFL Pharmaceuticals Deutschland GmbH
- IrelandAumseqa 55 mg film-coated tabletsSFL Pharmaceuticals Deutschland GmbH
- IcelandAumseqaSFL Pharmaceuticals Deutschland GmbH
- PolandAumseqaSFL Pharmaceuticals Deutschland GmbH
- SwedenAumseqa 55 mg Filmdragerad tablettSFL Pharmaceuticals Deutschland GmbH
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of CBG-MEB (Netherlands). 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/aae757ed-9028-422a-87ab-afdbeb3bc41a GET /v1/drugs/aae757ed-9028-422a-87ab-afdbeb3bc41a?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.
{
"form": "Filmomhulde tablet",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/aumseqa-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Aumolertinib",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp130780",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"IJZEROXIDE GEEL (E 172)",
"LACTOSE 0-WATER",
"MACROGOL",
"MACROGOL 3350",
"MAGNESIUMSTEARAAT (E 470b)",
"NATRIUMSTEARYLFUMARAAT",
"NATRIUMZETMEELGLYCOLAAT",
"POLYVINYLALCOHOL (E 1203)",
"TALK (E 553b)",
"TITAANDIOXIDE (E 171)"
],
"substances": [
"AUMOLERTINIBMESILAAT"
],
"leaflet_url": null,
"authorised_at": "2026/02/12",
"procedure_number": "EMEA/H/C/006069",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/25/2006",
"additional_monitoring": "Y"
}See everything about aumolertinib.
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.