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Poland· PL-100474555

Radelumin 1300 MBq/ml

A psma-1007 18f product containing psma-1007 (18f) solutio iniectabilis, registered in Poland by Abx Advanced Biochemical Compounds - Biomedizinische Forschungsreagenzien GmbH. The same ATC class is registered in 4 of our 19 countries.

ATC V09IX17

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedRadelumin 1300 MBq/mlATCV09IX17REGISTER NO.PL-100474555PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Psma-1007 18f is registered in 4 of 19 countries.

Countries holding a registration under ATC V09IX17 (psma-1007 18f), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 3 of them publish a price we can compare per daily dose

Psma-1007 18f · ATC V09IX17

4 / 19 countries

  • Belgiumprice
  • Netherlands
  • 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

URPL (Poland)
Active substance
PSMA-1007 (18F) solutio iniectabilis
Manufacturer
Abx Advanced Biochemical Compounds - Biomedizinische Forschungsreagenzien GmbH
Country
Poland (PL)
ATC code
V09IX17
ATC class
PSMA-1007 18F
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909991564339
  • gtin
    05909991564346

Regulatory notes

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

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of URPL (Poland). 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/91cf1da3-1733-4dc9-9c5c-6983bd9609b3
GET /v1/drugs/91cf1da3-1733-4dc9-9c5c-6983bd9609b3?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": "Roztwór do wstrzykiwań",
  "source": "urpl",
  "strength": "1300 MBq/ml",
  "packaging": "05909991564339 ¦ Lz ¦ 160306\n1 fiol. 15 ml\n05909991564346 ¦ Lz ¦ 160307\n1 fiol. 20 ml",
  "substance": "PSMA-1007 (18F) solutio iniectabilis 1300 MBq/ml",
  "common_name": "PSMA-1007 (18F) solutio iniectabilis",
  "pl_product_id": "100474555",
  "pozwolenie_nr": "28847",
  "auth_procedure": "MRP",
  "authorisation_validity": "2030-01-29"
}

See everything about psma-1007 18f.

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.