Netherlands· NL-d820f9cdd4bc
Nalador-500, poeder voor oplossing voor infusie 500 mcg
A sulproston product containing sulproston, registered in Netherlands by BModesto B.V.. The same ATC class is registered in 4 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Sulproston is registered in 4 of 19 countries.
Countries holding a registration under ATC G02AD05 (sulproston), 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
Sulproston · ATC G02AD05
4 / 19 countries
- Finlandprice
- Franceprice
- Netherlands
- Switzerlandprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- SULPROSTON
- Manufacturer
- BModesto B.V.
- Country
- Netherlands (NL)
- ATC code
- G02AD05
- ATC class
- Sulproston
- Defined daily dose
- 0.5 mg, P
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id132971//08996
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sulproston in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandNaladorSchering Oy
- SwitzerlandNalador, liofilizzatoFARMACEUTICA TEOFARMA SUISSE SA
- GermanyNalador-500Teofarma S.R.L.
- FranceNALADOR 500 microgrammes, lyophilisat pour usage parentéralTEOFARMA
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Austria · Nalador
- Germany · Nalador-500
- France · Nalador
- Hungary · Nalador
- Italy · Nalador
- Portugal · Nalador 500
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/6c95a31b-20e9-4214-9a1e-be51ba1a5e48 GET /v1/drugs/6c95a31b-20e9-4214-9a1e-be51ba1a5e48?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": "Poeder voor oplossing voor infusie",
"route": null,
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h08996_smpc.pdf",
"strength": null,
"atc_label": "Sulprostone",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg132971",
"excipients": [
"POVIDON K 17 (E 1201)",
"TROMETAMOL",
"ZOUTZUUR (E 507)"
],
"substances": [
"SULPROSTON"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h132971.pdf",
"authorised_at": "2024/04/05",
"procedure_number": null,
"dispensing_status": "Uitsluitend recept",
"registration_number": "132971//08996",
"additional_monitoring": "N"
}See everything about sulproston.
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.