United Kingdom· GB-APID-42781511000001102
Produodopa 2.4g/10ml / 120mg/10ml solution for infusion vials
A medicinal product containing foslevodopa + foscarbidopa, registered in United Kingdom by AbbVie Ltd.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Foslevodopa + Foscarbidopa
- Manufacturer
- AbbVie Ltd
- Country
- United Kingdom (GB)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 3
- gtin08054083024554
- gtin8054083024554
- gtin08054083028385
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Foslevodopa + foscarbidopa 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
- IrelandProduodopa 240 mg/ml + 12 mg/ml solution for infusionAbbVie Limited
- IcelandProduodopaAbbVie A/S
Authorised across Europe · EMA
The same active substance is authorised in 28 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
- Netherlands · Duodopa
- 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 NHS dm+d (United Kingdom). 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/84d0324a-d191-4ceb-b206-66aace0d7d25 GET /v1/drugs/84d0324a-d191-4ceb-b206-66aace0d7d25?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.
{
"apid": "42781511000001102",
"desc": "Produodopa 2.4g/10ml / 120mg/10ml solution for infusion vials (AbbVie Ltd)",
"form": "Solution for infusion",
"vpid": "42783711000001108",
"source": "dmd",
"vtm_id": "1332449001",
"strength": "240 mg",
"substance": "Foslevodopa + Foscarbidopa",
"ingredient": "Foslevodopa",
"supplier_code": "20741511000001103"
}See everything about foslevodopa + foscarbidopa.
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.