Back to search

United States· US:60267-705_4c4f587f-fb6f-4ce3-a09e-2a6a589b4d2b

Sodium Thiosulfate

A medicinal product containing sodium thiosulfate, registered in United States by Hope Pharmaceuticals.

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedSodium ThiosulfateATC—REGISTER NO.US:60267-705_4c4f587f…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
SODIUM THIOSULFATE
Manufacturer
Hope Pharmaceuticals
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    6026770550
    50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)
  • ndc11
    60267-705-50

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.

All sodium thiosulfate products

Authorised across Europe · EMA

The same active substance is authorised in 12 EEA countries. Names it is sold under:

  • Belgium · Thiosulfate De Sodium Sterop
  • 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 FDA National Drug Code directory (United States). 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/774c4ccf-8569-4c08-9911-57ef3516a4be
GET /v1/drugs/774c4ccf-8569-4c08-9911-57ef3516a4be?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.

{
  "route": "INTRAVENOUS",
  "source": "ndc",
  "strength": "250",
  "substance": "SODIUM THIOSULFATE",
  "productndc": "60267-705",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "NDA203923",
  "marketing_category": "NDA"
}

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.