Netherlands· NL-f8b54fd2c9cb
Ubretid 5 mg tabletten
A distigmine product containing distigminedibromide, registered in Netherlands by Euro Registratie Collectief B.V.. The same ATC class is registered in 7 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Distigmine is registered in 7 of 19 countries.
Countries holding a registration under ATC N07AA03 (distigmine), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 3 of them publish a price we can compare per daily dose
Distigmine · ATC N07AA03
7 / 19 countries
- Czechiaprice
- Finlandprice
- Germany
- Japan
- Netherlands
- Polandprice
- United Kingdom
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- DISTIGMINEDIBROMIDE
- Manufacturer
- Euro Registratie Collectief B.V.
- Country
- Netherlands (NL)
- ATC code
- N07AA03
- ATC class
- Distigmine
- Defined daily dose
- 5 mg, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id128191//07887
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Distigmine in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- PolandUbretidCHEPLAPHARM Arzneimittel GmbH
- CzechiaUBRETIDCHEPLAPHARM Arzneimittel GmbH, Greifswald
- United KingdomDistigmine bromide 5mg tabletsSpecial Order
- FinlandUbretidNycomed Austria GmbH
- GermanyUbretidCheplapharm Arzneimittel Gmbh
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Czechia · Ubretid
- Germany · Ubretid
- Poland · Ubretid
- Slovakia · Ubretid
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/3a9563c1-e3e1-499f-ad9c-b827ce1de44f GET /v1/drugs/3a9563c1-e3e1-499f-ad9c-b827ce1de44f?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": "Tablet",
"route": "Oraal gebruik",
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h07887_smpc.pdf",
"strength": null,
"atc_label": "Distigmine",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg128191",
"excipients": [
"LACTOSE 1-WATER",
"MAGNESIUMSTEARAAT (E 470b)",
"MAÏSZETMEEL",
"TALK (E 553b)",
"ZETMEEL, GEPREGELATINEERD"
],
"substances": [
"DISTIGMINEDIBROMIDE"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h128191.pdf",
"authorised_at": "2021/06/24",
"procedure_number": null,
"dispensing_status": "Uitsluitend recept",
"registration_number": "128191//07887",
"additional_monitoring": "N"
}See everything about distigmine.
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.