Netherlands· NL-b06e65c81d6e
Tivdak 40 mg poeder voor concentraat voor oplossing voor infusie
A tisotumab vedotin product containing tisotumab vedotin, registered in Netherlands by Genmab A/S. The same ATC class is registered in 10 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Tisotumab vedotin is registered in 10 of 19 countries.
Countries holding a registration under ATC L01FX23 (tisotumab vedotin), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 6 of them publish a price we can compare per daily dose
Tisotumab vedotin · ATC L01FX23
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- TISOTUMAB VEDOTIN
- Manufacturer
- Genmab A/S
- Country
- Netherlands (NL)
- ATC code
- L01FX23
- ATC class
- Tisotumab vedotin
- Defined daily dose
- 6.67 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/25/1911
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Tisotumab vedotin in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumTivdak 40 mgGenmab
- CzechiaTIVDAKGENMAB A/S, Valby
- SpainTIVDAK 40 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONGenmab A/S
- FinlandTivdakGenmab A/S
- United KingdomTivdak 40mg powder for concentrate for solution for infusion vialsGenmab A/S
- IrelandTivdak 40 mg powder for concentrate for solution for infusionGenmab A/S
- IcelandTivdakGenmab A/S
- Japanチソツマブ ベドチン(遺伝子組換え)ジェンマブ
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Tivdak
- Liechtenstein · Tivdak
- Norway · Tivdak
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/fdfffe28-3940-4afc-bddf-9965c5d9c8f5 GET /v1/drugs/fdfffe28-3940-4afc-bddf-9965c5d9c8f5?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": "Poeder voor concentraat voor oplossing voor infusie",
"route": "Intraveneus gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/tivdak-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Tisotumab Vedotin",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp132887",
"excipients": [
"HISTIDINE, (L-)",
"HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
"MANNITOL (D-) (E 421)",
"SACCHAROSE"
],
"substances": [
"TISOTUMAB VEDOTIN"
],
"leaflet_url": null,
"authorised_at": "2025/03/28",
"procedure_number": "EMEA/H/C/005363",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/25/1911",
"additional_monitoring": "Y"
}See everything about tisotumab vedotin.
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.