Netherlands· NL-df7a2343139e
Enjaymo 50mg/ml, oplossing voor infusie
A sutimlimab product containing sutimlimab, registered in Netherlands by Recordati Rare Diseases. The same ATC class is registered in 9 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Sutimlimab is registered in 9 of 19 countries.
Countries holding a registration under ATC L04AJ04 (sutimlimab), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 7 of them publish a price we can compare per daily dose
Sutimlimab · ATC L04AJ04
9 / 19 countries
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- SUTIMLIMAB
- Manufacturer
- Recordati Rare Diseases
- Country
- Netherlands (NL)
- ATC code
- L04AJ04
- ATC class
- Sutimlimab
- Defined daily dose
- 0.46 g, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/22/1687
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sutimlimab in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceENJAYMO 50 mg/ml, solution pour perfusionRECORDATI RARE DISEASES
- SwitzerlandEnjaymo 1100 mg/22 ml, InfusionslösungRECORDATI AG
- CzechiaENJAYMORecordati Rare Diseases, Puteaux
- FinlandEnjaymoRecordati Rare Diseases
- IrelandEnjaymo 50 mg/mL solution for infusionRecordati Rare Diseases
- IcelandEnjaymoRecordati Rare Diseases
- Japanスチムリマブ(遺伝子組換え)レコルダティ・レア・ディジーズ・ジャパン
- NorwayEnjaymoRecordati Rare Diseases
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Enjaymo
- Liechtenstein · Enjaymo
- Norway · Enjaymo
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/b108f1ad-cf87-42a6-990c-90e9261c6aa2 GET /v1/drugs/b108f1ad-cf87-42a6-990c-90e9261c6aa2?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/enjaymo-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Sutimlimab",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp129098",
"excipients": [
"DINATRIUMWATERSTOFFOSFAAT 7-WATER (E 339)",
"NATRIUMCHLORIDE",
"NATRIUMDIWATERSTOFFOSFAAT 1-WATER (E 339)",
"POLYSORBAAT 80 (E 433)",
"WATER VOOR INJECTIE"
],
"substances": [
"SUTIMLIMAB"
],
"leaflet_url": null,
"authorised_at": "2022/11/15",
"procedure_number": "EMEA/H/C/005776",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/22/1687",
"additional_monitoring": "Y"
}See everything about sutimlimab.
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.