Spain· ES:91176
KINPARLEV 6 MG/24 H PARCHE TRANSDERMICO EFG
A medicinal product containing rotigotina, registered in Spain by Orion Corporation.
Checked against AEMPS CIMA (Spain) on
Informational only — not a medical device.
The record
At a glance
AEMPS CIMA (Spain)- Active substance
- rotigotina
- Manufacturer
- Orion Corporation
- Country
- Spain (ES)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- AEMPS CIMA (Spain)
- Last checked
- June 8, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Rotigotina in 17 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaNEUPROUCB Pharma SA, Brusel
- BelgiumLeganto 6 mg/24 hUCB
- ItalyNEUPROUCB PHARMA S.A.
- United StatesNeuproUCB, Inc.
- PolandNeuproUCB Pharma S.A.
- NetherlandsNeupro 6 mg/24 h pleister voor transdermaal gebruikUCB Pharma S.A.
- United KingdomNeupro 1mg/24hours transdermal patchesUCB Pharma Ltd
- FinlandKinparlevOrion Corporation
Authorised across Europe · EMA
The same active substance is authorised in 15 EEA countries. Names it is sold under:
- Austria · Kinparlev, Rotigotin Gebro
- Germany · Rotigotin Luye, Rotigotin Neuraxpharm
- Denmark · Kinparlev, Rotigotine Medical Valley
- Finland · Kinparlev, Rotigotine Medical Valley
- France · Rotigotine Arrow
- Greece · Kinparlev
- Iceland · Neupro, Rotigotine Medical Valley
- Italy · Rotigotina Doc
- Liechtenstein · Neupro
- Luxembourg · Rotigotin Luye
- Netherlands · Rotigotine Medical Valley, Rotigotine Xiromed
- Norway · Kinparlev, Neupro
- Portugal · Kinparlev, Rotigotina Generis
- Romania · Kinparlev
- Sweden · Kinparlev, Rotigotine Medical Valley
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 AEMPS CIMA (Spain). 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/e8ea03c5-1ae3-4778-9458-54a624e0b82c GET /v1/drugs/e8ea03c5-1ae3-4778-9458-54a624e0b82c?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.
{
"cpresc": "Medicamento Sujeto A Prescripción Médica",
"estado": "{\"aut\":1780487288000}",
"nregistro": "91176",
"substance": "rotigotina"
}See everything about rotigotina.
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.