Back to search

Germany· DE-A57-a410de6cf2f12e1f

Ioflupan (123i) Rotop

A medicinal product containing ioflupane (123i), registered in Germany by Rotop Radiopharmacy Gmbh.

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedIoflupan (123i) RotopATC—REGISTER NO.DE-A57-a410de6cf2f12e…PACKS LISTED0CHECKEDSeptember 30, 2026

The record

At a glance

EMA Article 57 (European Union)
Active substance
Ioflupane (123i)
Manufacturer
Rotop Radiopharmacy Gmbh
Country
Germany (DE)
ATC code
—
Reimbursed
Not published by this register
Source register
EMA Article 57 (European Union)
Last checked
September 30, 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 (123i) in 9 other countries

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

All ioflupane (123i) 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
  • Finland · Joflupaani (123i) Rotop
  • France · Ioflupane (123i) Rotop
  • United Kingdom (Northern Ireland) · Datscan, 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 EMA Article 57 (European Union). 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/3393b76e-5de2-42ef-8fef-ff113b4ed392
GET /v1/drugs/3393b76e-5de2-42ef-8fef-ff113b4ed392?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.

{
  "pzn": null,
  "route": "Intravenous Use",
  "source": "ema_art57_de",
  "ma_number": null,
  "substance": "Ioflupane (123i)",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}

See everything about ioflupane (123i).

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.