Finland· FI-REL-REL2182
Nalador
A sulproston product containing sulprostone, registered in Finland by Schering Oy. The same ATC class is registered in 4 of our 19 countries.
Checked against Fimea (Finland) 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: Finland, from Fimea (Finland)
- 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
Fimea (Finland)- Active substance
- Sulprostone
- Manufacturer
- Schering Oy
- Country
- Finland (FI)
- ATC code
- G02AD05
- ATC class
- Sulproston
- Defined daily dose
- 0.5 mg, P
- Reimbursed
- Not published by this register
- Source register
- Fimea (Finland)
- Last checked
- September 27, 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
Sulproston in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsNalador-500, poeder voor oplossing voor infusie 500 mcgBModesto B.V.
- 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 7 EEA countries. Names it is sold under:
- Austria · Nalador
- Germany · Nalador-500
- France · Nalador
- Hungary · Nalador
- Italy · Nalador
- Netherlands · 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 Fimea (Finland). 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/ea80e3db-e7ac-4824-89fd-c39f48ae422c GET /v1/drugs/ea80e3db-e7ac-4824-89fd-c39f48ae422c?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.
{
"ddd": "0.5",
"form": "infuusiokuiva-aine, liuosta varten",
"route": null,
"ddd_unit": "mg",
"strength": "0.5 mg",
"atc_label": "sulprostoni",
"ma_number": "9552",
"auth_status": "Myyntilupa peruuntunut",
"eu_ma_number": null,
"fimea_rel_id": "REL2182",
"authorised_at": "1987-11-04"
}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.