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Belgium· BE-AMP-SAM186173-00

LeukoScan 0,31 mg

A other diagnostic agents product containing sulesomab, registered in Belgium by Immunomedics Europe. The same ATC class is registered in 11 of our 19 countries.

ATC V04CX

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedLeukoScan 0,31 mgATCV04CXREGISTER NO.BE-AMP-SAM186173-00PACKS LISTED0CHECKEDSeptember 26, 2026

Where it is registered

Sulesomab is registered in 11 of 19 countries.

Countries holding a registration under ATC V04CX (other diagnostic agents), each read from that country’s own register.

  • This record: Belgium, from FAMHP / AFMPS (Belgium)
  • 7 of them publish a price we can compare per daily dose

Sulesomab · ATC V04CX

11 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Sulesomab
Manufacturer
Immunomedics Europe
Country
Belgium (BE)
ATC code
V04CX
ATC class
Other diagnostic agents
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 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

Sulesomab in 2 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All sulesomab products

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/e6f183a2-525c-4441-883c-ef37cdb3aa60
GET /v1/drugs/e6f183a2-525c-4441-883c-ef37cdb3aa60?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": "Powder for solution for injection",
  "source": "afmps",
  "status": "REVOKED",
  "name_en": "LeukoScan 0,31 mg",
  "name_fr": "LeukoScan 0,31 mg",
  "name_nl": "LeukoScan 0,31 mg",
  "amp_code": "SAM186173-00",
  "strengths": [
    "0.3100"
  ],
  "pack_count": 1,
  "substances": [
    "Sulesomab"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Other Diagnostic Agents",
  "authorisation_numbers": [
    "EU/1/97/032/001"
  ]
}

See everything about sulesomab.

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.