Netherlands· NL-586619dff2a7
Duodopa 240 mg/ml + 12 mg/ml oplossing voor infusie
A foslevodopa und decarboxylasehemmer product containing foscarbidopa x-water + foslevodopa, registered in Netherlands by AbbVie B.V.. The same ATC class is registered in 8 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Foslevodopa und decarboxylasehemmer is registered in 8 of 19 countries.
Countries holding a registration under ATC N04BA07 (foslevodopa und decarboxylasehemmer), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 5 of them publish a price we can compare per daily dose
Foslevodopa und decarboxylasehemmer · ATC N04BA07
8 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- FOSCARBIDOPA X-WATER + FOSLEVODOPA
- Manufacturer
- AbbVie B.V.
- Country
- Netherlands (NL)
- ATC code
- N04BA07
- ATC class
- Foslevodopa und Decarboxylasehemmer
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id128752
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Foslevodopa und decarboxylasehemmer in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CanadaVYALEVABBVIE CORPORATION
- CzechiaDUODOPA SCAbbVie s.r.o., Praha
- GermanyProduodopaAbbvie Deutschland Gmbh & Co. Kg
- SpainDUODOPA 240 MG/ML + 12 MG/ML SOLUCION PARA PERFUSIONAbbvie Spain, S.L.U.
- FinlandProduodopaAbbVie Oy
- FranceSCYOVA 240 mg/mL + 12 mg/mL, solution pour perfusionABBVIE
- United KingdomProduodopa 2.4g/10ml / 120mg/10ml solution for infusion vialsAbbVie Ltd
- IrelandProduodopa 240 mg/ml + 12 mg/ml solution for infusionAbbVie Limited
Authorised across Europe · EMA
The same active substance is authorised in 27 EEA countries. Names it is sold under:
- Austria · Produodopa
- Belgium · Produodopa
- Bulgaria · Продуодопа
- Cyprus · Produodopa
- Czechia · Duodopa Sc
- Germany · Produodopa®
- Denmark · Duodopa
- Estonia · Produodopa
- Spain · Duodopa
- Finland · Produodopa
- France · Scyova
- Greece · Produodopa
- Croatia · Produodopa
- Hungary · Produodopa
- Ireland · Produodopa
- Iceland · Produodopa
- Italy · Duodopa
- Liechtenstein · Produodopa
- Lithuania · Duodopa
- Luxembourg · Produodopa
- Norway · Produodopa
- Poland · Produodopa
- Portugal · Duodopa
- Romania · Produodopa
- Sweden · Produodopa
- Slovenia · Produodopa
- Slovakia · Duodopa Sc
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/93331cf1-7b6d-4bef-86b9-9be6d077fe1a GET /v1/drugs/93331cf1-7b6d-4bef-86b9-9be6d077fe1a?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": "Subcutaan gebruik",
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h128752_smpc.pdf",
"strength": null,
"atc_label": "Foslevodopa and Decarboxylase Inhibitor",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg128752",
"excipients": [
"NATRIUMHYDROXIDE (E 524)",
"STIKSTOF (HEAD SPACE) (E 941)",
"WATER VOOR INJECTIE",
"ZOUTZUUR (E 507)"
],
"substances": [
"FOSCARBIDOPA X-WATER",
"FOSLEVODOPA"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h128752.pdf",
"authorised_at": "2022/11/07",
"procedure_number": "SE/H/0415/003",
"dispensing_status": "Uitsluitend recept",
"registration_number": "128752",
"additional_monitoring": "N"
}See everything about foslevodopa und decarboxylasehemmer.
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.