Iceland· IS-EU/1/22/1703/001

Pluvicto

A lutetium (177lu) oxodotreotide product containing lutetium (177lu) vipivotide tetraxetan, registered in Iceland by Novartis Europharm Limited*. The same ATC class is registered in 11 of our 19 countries.

ATC V10XX04

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedPluvictoATCV10XX04REGISTER NO.IS-EU/1/22/1703/001PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Lutetium (177lu) oxodotreotide is registered in 11 of 19 countries.

Countries holding a registration under ATC V10XX04 (lutetium (177lu) oxodotreotide), each read from that country’s own register.

  • This record: Iceland, from Icelandic Medicines Agency (Iceland)
  • 7 of them publish a price we can compare per daily dose

Lutetium (177lu) oxodotreotide · ATC V10XX04

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

Icelandic Medicines Agency (Iceland)
Active substance
Lutetium (177Lu) vipivotide tetraxetan
Manufacturer
Novartis Europharm Limited*
Country
Iceland (IS)
ATC code
V10XX04
ATC class
Lutetium (177Lu) oxodotreotide
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 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.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Icelandic Medicines Agency (Iceland). 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/6156dd33-b544-4fe0-9ad9-4d9bc0d17e7c
GET /v1/drugs/6156dd33-b544-4fe0-9ad9-4d9bc0d17e7c?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": "Stungulyf/innrennslislyf, lausn",
  "source": "lyfjastofnun",
  "atc_raw": "V10XX04",
  "marketed": false,
  "strength": "1000 MBq/ml",
  "ma_number": "EU/1/22/1703/001",
  "substance": "Lutetium (177Lu) vipivotide tetraxetan",
  "other_info": "Markaðssetning á Íslandi er háð því að Lyfjastofnun hafi staðfest að sérstök skilyrði er varða öryggi og verkun við notkun lyfsins séu uppfyllt.",
  "legal_status": "(R) Lyfseðilsskylt\r\n(H) Sjúkrahúsmerkt",
  "ma_issued_serial": "44904"
}

See everything about lutetium (177lu) oxodotreotide.

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.