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Belgium· BE-AMP-SAM660909-00

Monlutenca 40 GBq/ml

A other therapeutic radiopharmaceuticals product containing lutetium (lu-177) chloride, registered in Belgium by Curium Romania. The same ATC class is registered in 8 of our 19 countries.

ATC V10X

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedMonlutenca 40 GBq/mlATCV10XREGISTER NO.BE-AMP-SAM660909-00PACKS LISTED0CHECKEDSeptember 26, 2026

Where it is registered

Lutetium (lu-177) chloride is registered in 8 of 19 countries.

Countries holding a registration under ATC V10X (other therapeutic radiopharmaceuticals), each read from that country’s own register.

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

Lutetium (lu-177) chloride · ATC V10X

8 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Polandprice
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
Lutetium (Lu-177) Chloride
Manufacturer
Curium Romania
Country
Belgium (BE)
ATC code
V10X
ATC class
OTHER THERAPEUTIC RADIOPHARMACEUTICALS
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

Lutetium (lu-177) chloride in 2 other countries

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

All lutetium (lu-177) chloride 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/2cbcbf4a-e2bb-42af-ade7-eca0fc777fa4
GET /v1/drugs/2cbcbf4a-e2bb-42af-ade7-eca0fc777fa4?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": "Radiopharmaceutical precursor, solution",
  "source": "afmps",
  "status": "AUTHORIZED",
  "name_en": "Monlutenca 40 GBq/ml",
  "name_fr": "Monlutenca 40 GBq/ml",
  "name_nl": "Monlutenca 40 GBq/ml",
  "amp_code": "SAM660909-00",
  "strengths": [
    "40.0000",
    "40.0000",
    "40.0000"
  ],
  "pack_count": 3,
  "substances": [
    "Lutetium (Lu-177) Chloride"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Other Therapeutic Radiopharmaceuticals",
  "authorisation_numbers": [
    "BE660909"
  ]
}

See everything about lutetium (lu-177) chloride.

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.