Netherlands· NL-0e147d710684
Libtayo 350 mg concentraat voor oplossing voor infusie
A cemiplimab product containing cemiplimab, registered in Netherlands by Regeneron Ireland Designated Activity Company. The same ATC class is registered in 12 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Cemiplimab is registered in 12 of 19 countries.
Countries holding a registration under ATC L01FF06 (cemiplimab), 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
Cemiplimab · ATC L01FF06
12 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- CEMIPLIMAB
- Manufacturer
- Regeneron Ireland Designated Activity Company
- Country
- Netherlands (NL)
- ATC code
- L01FF06
- ATC class
- Cemiplimab
- Defined daily dose
- 16.7 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/19/1376
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
17 interactions on record for cemiplimab.
Graded by severity as the source publishes them — 17 moderate. 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
Cemiplimab · interactions on record
17 records
- 17 moderate
Most severe, free to view
- PrednisoloneA07EA01moderate
- HydrocortisoneA07EA02moderate
- PrednisoneA07EA03moderate
- BetamethasoneA07EA04moderate
- 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
Cemiplimab in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceLIBTAYO 350 mg, solution à diluer pour perfusionREGENERON IRELAND DESIGNATED ACTIVITY COMPANY (IRLANDE)
- NorwayLibtayoAbacus Medicine A/S
- FinlandLIBTAYOOrifarm Oy
- SpainLIBTAYO 350 MG CONCENTRADO PARA SOLUCION PARA PERFUSIONRegeneron Ireland Designated Activity Company
- United StatesLIBTAYORegeneron Pharmaceuticals, Inc.
- BelgiumLibtayo 350 mgRegeneron Ireland Designated Activity Company (DAC)
- IrelandLIBTAYO 350 mg Concentrate for solution for infusionRegeneron Ireland U.C.
- IcelandLibtayoRegeneron Ireland Designated Activity Company
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Libtayo
- Liechtenstein · Libtayo
- Norway · Libtayo
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/0cfe02c8-725d-40b5-9ea3-ba1965ab6915 GET /v1/drugs/0cfe02c8-725d-40b5-9ea3-ba1965ab6915?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": "Concentraat voor oplossing voor infusie",
"route": "Intraveneus gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/libtayo-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Cemiplimab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp122801",
"excipients": [
"HISTIDINE, (L-)",
"HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
"POLYSORBAAT 80 (E 433)",
"PROLINE, (L-)",
"SACCHAROSE",
"WATER VOOR INJECTIE"
],
"substances": [
"CEMIPLIMAB"
],
"leaflet_url": null,
"authorised_at": "2019/06/28",
"procedure_number": "EMEA/H/C/004844",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/19/1376",
"additional_monitoring": "Y"
}See everything about cemiplimab.
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.