Back to search

United Kingdom· GB-APID-39416611000001107

DaTSCAN [I-123] 370MBq/5ml solution for injection vials

A medicinal product containing ioflupane [i-123], registered in United Kingdom by GE Healthcare Ltd.

Checked against NHS dm+d (United Kingdom) on

Informational only — not a medical device.

SOURCE REGISTER · GBNHS dm+d (United Kingdom)normalisedDaTSCAN [I-123] 370MBq/5ml solution f…ATC—REGISTER NO.GB-APID-3941661100000…PACKS LISTED0CHECKEDSeptember 13, 2026

The record

At a glance

NHS dm+d (United Kingdom)
Active substance
Ioflupane [I-123]
Manufacturer
GE Healthcare Ltd
Country
United Kingdom (GB)
ATC code
—
Reimbursed
Not published by this register
Source register
NHS dm+d (United Kingdom)
Last checked
September 13, 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

Ioflupane [i-123] in 9 other countries

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

All ioflupane [i-123] products

Authorised across Europe · EMA

The same active substance is authorised in 15 EEA countries. Names it is sold under:

  • Austria · Ioflupan (123i) Rotop
  • Belgium · Ioflupan (123i) Rotop, Ioflupane (123i) Rotop
  • Czechia · Joflupan (123i) Rotop
  • Germany · Ioflupan (123i) Rotop
  • Finland · Joflupaani (123i) Rotop
  • France · Ioflupane (123i) Rotop
  • Iceland · Datscan, Striascan
  • Italy · Ioflupane (123i) Rotop
  • Liechtenstein · Datscan
  • Luxembourg · Ioflupane (123i) Rotop
  • Netherlands · Joflupaan (123i) Rotop
  • Norway · Datscan, Ioflupane (123i) Rotop
  • Poland · Ioflupane (123i) Rotop
  • Portugal · Ioflupano (123i) Rotop
  • Sweden · Ioflupan (123i) Rotop

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 NHS dm+d (United Kingdom). 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/9225b20d-7fa0-4d61-89f2-d19bfea8e4f2
GET /v1/drugs/9225b20d-7fa0-4d61-89f2-d19bfea8e4f2?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.

{
  "apid": "39416611000001107",
  "desc": "DaTSCAN [I-123] 370MBq/5ml solution for injection vials (GE Healthcare Ltd)",
  "form": "Solution for injection",
  "vpid": "39418011000001101",
  "source": "dmd",
  "vtm_id": "39417211000001107",
  "strength": "74 MBq",
  "substance": "Ioflupane [I-123]",
  "ingredient": "Ioflupane [I-123]",
  "supplier_code": "11269611000001107"
}

See everything about ioflupane [i-123].

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.