Ireland· IE-PA-EU/1/05/331/10-12,32-37
Neupro
A dopamine agonists product containing rotigotine, registered in Ireland by Schwarz Pharma Limited.
Checked against HPRA (Ireland) on
Informational only — not a medical device.
The record
At a glance
HPRA (Ireland)- Active substance
- Rotigotine
- Manufacturer
- Schwarz Pharma Limited
- Country
- Ireland (IE)
- ATC code
- N04BC
- ATC class
- Dopamine agonists
- Reimbursed
- Not published by this register
- Source register
- HPRA (Ireland)
- Last checked
- September 28, 2026
Packs & prices · 1
- ie_pa_numberEU/1/05/331/10-12,32-37
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Rotigotine in 17 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomNeupro 1mg/24hours transdermal patchesUCB Pharma Ltd
- CzechiaNEUPROUCB Pharma SA, Brusel
- SpainDARIANTE 1 MG/24 HORAS PARCHES TRANSDÉRMICOS EFGExeltis Healthcare S.L.
- FinlandKinparlevOrion Corporation
- NetherlandsKinparlev 1 mg/24 uur pleister voor transdermaal gebruikOrion Corporation
- BelgiumLegantoUCB
- SwedenKinparlev 1 mg/24 timmar DepotplåsterOrion Corporation
- United StatesNeuproUCB, Inc.
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Kinparlev, Rotigotin Gebro
- Germany · Rotigotin Luye, Rotigotin Neuraxpharm
- Denmark · Kinparlev, Rotigotine Medical Valley
- Spain · Dariante
- 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 HPRA (Ireland). 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/b338d603-e28a-4b4a-b73a-f1e1d1622274 GET /v1/drugs/b338d603-e28a-4b4a-b73a-f1e1d1622274?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": "Transdermal patch",
"routes": null,
"source": "hpra",
"atc_all": [
"N04BC"
],
"strength": null,
"pa_number": "EU/1/05/331/10-12,32-37",
"substances": [
"Rotigotine"
],
"legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
"market_info": "Unknown",
"authorised_at": "15/02/2006",
"dispensing_status": "Product subject to prescription which may not be renewed (A)",
"registration_status": "AU",
"supply_legal_status": "Supply through pharmacies only",
"interchangeable_code": null
}See everything about rotigotine.
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.