Netherlands· NL-676ed4a5e4b9
Tecartus 0.4-2.0 x 10^8 cellen, dispersie voor infusie
A brexucabtagene autoleucel product containing brexucabtageen autoleucel, registered in Netherlands by Kite Pharma EU B.V.. The same ATC class is registered in 13 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Brexucabtagene autoleucel is registered in 13 of 19 countries.
Countries holding a registration under ATC L01XL06 (brexucabtagene autoleucel), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 8 of them publish a price we can compare per daily dose
Brexucabtagene autoleucel · ATC L01XL06
13 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- BREXUCABTAGEEN AUTOLEUCEL
- Manufacturer
- Kite Pharma EU B.V.
- Country
- Netherlands (NL)
- ATC code
- L01XL06
- ATC class
- Brexucabtagene autoleucel
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/20/1492
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
82 interactions on record for brexucabtagene autoleucel.
Graded by severity as the source publishes them — 51 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Brexucabtagene autoleucel · interactions on record
82 records
- 51 severe
- 31 moderate
Most severe, free to view
- PrednisoloneA07EA01severe
- HydrocortisoneA07EA02severe
- PrednisoneA07EA03severe
- BetamethasoneA07EA04severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Brexucabtagene autoleucel in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesTECARTUSKite Pharma, Inc.
- CanadaTECARTUSGILEAD SCIENCES CANADA INC
- SpainTECARTUS 0,4 - 2 x 10e8 CELULAS DISPERSION PARA PERFUSIONKite Pharma Eu B.V.
- FinlandTecartusKite Pharma EU B.V.
- BelgiumTecartus 0.4 10*8 cells/ml - 2 10*8 cells/mlKite Pharma EU
- IcelandTecartusKite Pharma EU B.V.
- NorwayTecartusKite Pharma EU B.V.
- PolandTecartusKite Pharma EU B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tecartus
- Liechtenstein · Tecartus
- Norway · Tecartus
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 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/7960dd0a-0ca1-43be-9aac-2df8874159d9 GET /v1/drugs/7960dd0a-0ca1-43be-9aac-2df8874159d9?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": "Oplossing voor infusie",
"route": "Intraveneus gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/tecartus-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Brexucabtagene Autoleucel",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp126203",
"excipients": [
"ADENOSINE",
"CALCIUMCHLORIDE 2-WATER (E 509)",
"DEXTRAAN 40",
"DIMETHYLSULFOXIDE",
"GLUCOSE 0-WATER",
"GLUTATHION (L-)",
"HUMAAN ALBUMINE",
"KALIUMCHLORIDE (E 508)",
"KALIUMDIWATERSTOFFOSFAAT 0-WATER (E 340)",
"KALIUMHYDROXIDE (E 525)",
"KALIUMWATERSTOFCARBONAAT (E 501 (II))",
"LACTOBIONZUUR",
"MAGNESIUMCHLORIDE 6-WATER (E 511)",
"MANNITOL (D-) (E 421)",
"N-2-HYDROXYETHYLPIPERAZINE-N'-2-ETHAANSULFONZUUR",
"NATRIUMCHLORIDE",
"NATRIUMHYDROXIDE (E 524)",
"SACCHAROSE",
"WATER VOOR INJECTIE"
],
"substances": [
"BREXUCABTAGEEN AUTOLEUCEL"
],
"leaflet_url": null,
"authorised_at": "2020/12/14",
"procedure_number": "EMEA/H/C/005102",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/20/1492",
"additional_monitoring": "Y"
}See everything about brexucabtagene autoleucel.
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.