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Belgium· BE-AMP-SAM154296-00

Magnevist 0,5 mmol/ml

A gadopentetsäure product containing gadopentetate dimeglumine, registered in Belgium by Bayer. The same ATC class is registered in 3 of our 19 countries.

ATC V08CA01

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedMagnevist 0,5 mmol/mlATCV08CA01REGISTER NO.BE-AMP-SAM154296-00PACKS LISTED2CHECKEDSeptember 26, 2026

Where it is registered

Gadopentetsäure is registered in 3 of 19 countries.

Countries holding a registration under ATC V08CA01 (gadopentetsäure), each read from that country’s own register.

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

Gadopentetsäure · ATC V08CA01

3 / 19 countries

  • Belgiumprice
  • Canada
  • Finlandprice
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
Gadopentetate Dimeglumine
Manufacturer
Bayer
Country
Belgium (BE)
ATC code
V08CA01
ATC class
Gadopentetsäure
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 2

  • be_apb
    1414598
  • be_apb
    0749069

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Gadopentetsäure in 3 other countries

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

All gadopentetsäure products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Germany · Magnevist
  • United Kingdom (Northern Ireland) · Magnevist

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/fc4caf7b-fe43-412c-990f-8c11c83c8d50
GET /v1/drugs/fc4caf7b-fe43-412c-990f-8c11c83c8d50?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": "Solution for injection",
  "source": "afmps",
  "status": "REVOKED",
  "name_en": "Magnevist 0,5 mmol/ml",
  "name_fr": "Magnevist 0,5 mmol/ml",
  "name_nl": "Magnevist 0,5 mmol/ml",
  "amp_code": "SAM154296-00",
  "strengths": [
    "469.0000"
  ],
  "pack_count": 1,
  "substances": [
    "Gadopentetate Dimeglumine"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Gadopentetic Acid",
  "authorisation_numbers": [
    "BE154296"
  ]
}

See everything about gadopentetsäure.

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.