Belgium· BE-AMP-SAM063847-00
Gammadyn Soufre
A medicinal product containing sodium thiosulfate, registered in Belgium by Unda.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Sodium Thiosulfate
- Manufacturer
- Unda
- Country
- Belgium (BE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 1
- be_apb0682583
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium thiosulfate 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
- 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.
- SwedenNatriumtiosulfat Hope 250 mg/ml Injektionsvätska, lösningHope Pharmaceuticals Limited
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Germany · Natriumthiosulfat
- 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 FAMHP / AFMPS (Belgium). 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/d8d2e147-6b1b-49a4-97c5-c6999fa401ab GET /v1/drugs/d8d2e147-6b1b-49a4-97c5-c6999fa401ab?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": "Sublingual solution",
"source": "afmps",
"status": "REVOKED",
"name_en": "Gammadyn Soufre",
"name_fr": "Gammadyn Soufre",
"name_nl": "Gammadyn Soufre",
"amp_code": "SAM063847-00",
"strengths": [
"0.3000",
"0.3000"
],
"pack_count": 1,
"substances": [
"Sodium Thiosulfate"
],
"medicine_type": "ALLOPATHIC",
"atc_description": null,
"authorisation_numbers": [
"0341S 0194F011"
]
}See everything about sodium thiosulfate.
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.