Germany· DE-A57-e497a11477323020
Natriumthiosulfat
A medicinal product containing sodium thiosulfate pentahydrate, registered in Germany by Dr. Franz Köhler Chemie Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Sodium Thiosulfate Pentahydrate
- Manufacturer
- Dr. Franz Köhler Chemie Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 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
Sodium thiosulfate pentahydrate in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomPedmarqsi 8g/100ml solution for infusion vialsNorgine Pharmaceuticals Ltd
- CanadaSEACALPHYXSEAFORD PHARMACEUTICALS INC
- BelgiumGammadyn SoufreUnda
- Japanチオ硫酸ナトリウム水和物
- United StatesPEDMARKFennec Pharmaceuticals Inc.
- CzechiaNATRIUMTHIOSULFAT 10%
- IrelandPedmarqsi 80 mg/mL solution for infusionNorgine B.V.
- NetherlandsNatriumthiosulfaat Hope 250 mg/ml, oplossing voor injectieHope Pharmaceuticals, Ltd.
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Belgium · Thiosulfate De Sodium Sterop
- France · Oligosol
- United Kingdom (Northern Ireland) · Pedmarqsi, Sodium Thiosulfate Hope Pharmaceuticals
- Ireland · Sodium Thiosulfate Hope Pharmaceuticals
- Iceland · Pedmarqsi
- Italy · Sodio Tiosolfato Monico, Sodio Tiosolfato S.A.L.F.
- Liechtenstein · Pedmarqsi
- Luxembourg · Oligosol
- Netherlands · Natriumthiosulfaat Hope
- Norway · Pedmarqsi
- Sweden · Natriumtiosulfat Hope
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 EMA Article 57 (European Union). 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/cf4a0eb8-885d-4dbc-809c-bfbd6dc7b90c GET /v1/drugs/cf4a0eb8-885d-4dbc-809c-bfbd6dc7b90c?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.
{
"pzn": null,
"route": "Intravenous Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Sodium Thiosulfate Pentahydrate",
"atc_from_source": null,
"authorisation_country": "Germany"
}See everything about sodium thiosulfate pentahydrate.
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.