Netherlands· NL-025ee806f0e4
Perfan, concentraat voor oplossing voor infusie 5 mg/ml
A enoximone product containing enoximon, registered in Netherlands by Eureco-Pharma B.V.. The same ATC class is registered in 4 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Enoximone is registered in 4 of 19 countries.
Countries holding a registration under ATC C01CE03 (enoximone), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 1 of them publish a price we can compare per daily dose
Enoximone · ATC C01CE03
4 / 19 countries
- Franceprice
- Germany
- Netherlands
- United Kingdom
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- ENOXIMON
- Manufacturer
- Eureco-Pharma B.V.
- Country
- Netherlands (NL)
- ATC code
- C01CE03
- ATC class
- Enoximone
- Defined daily dose
- 1 g, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id135214//13343
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Enoximone in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyPerfanCarinopharm Gmbh
- FrancePERFANE 100 mg/20 ml, solution injectable à diluer pour voie I.V.CARINOPHARM (ALLEMAGNE)
- United KingdomPerfan 100mg/20ml solution for injection ampoulesMacure Pharma UK Ltd
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Germany · Perfan
- France · Perfane
- United Kingdom (Northern Ireland) · Perfan
- Italy · Perfan
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/f41b9b42-93c4-48ab-a2d3-a65dc1bef728 GET /v1/drugs/f41b9b42-93c4-48ab-a2d3-a65dc1bef728?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": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h13343_smpc.pdf",
"strength": null,
"atc_label": "Enoximone",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg135214",
"excipients": [
"ETHANOL",
"NATRIUMHYDROXIDE (E 524)",
"PROPYLEENGLYCOL (E 1520)",
"WATER VOOR INJECTIE"
],
"substances": [
"ENOXIMON"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h135214.pdf",
"authorised_at": "2025/07/07",
"procedure_number": null,
"dispensing_status": "Uitsluitend recept",
"registration_number": "135214//13343",
"additional_monitoring": "N"
}See everything about enoximone.
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.