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Spain· ES:83803

TETROFOSMINA ROTOP 0,23 MG EQUIPO DE REACTIVOS PARA PREPARACION RADIOOFARMACEUTICA EFG

A medicinal product containing tetrofosmina, registered in Spain by Rotop Pharmaka Gmbh.

Checked against AEMPS CIMA (Spain) on

Informational only — not a medical device.

SOURCE REGISTER · ESAEMPS CIMA (Spain)normalisedTETROFOSMINA ROTOP 0,23 MG EQUIPO DE …ATC—REGISTER NO.ES:83803PACKS LISTED0CHECKEDSeptember 12, 2026

The record

At a glance

AEMPS CIMA (Spain)
Active substance
tetrofosmina
Manufacturer
Rotop Pharmaka Gmbh
Country
Spain (ES)
ATC code
—
Reimbursed
Not published by this register
Source register
AEMPS CIMA (Spain)
Last checked
September 12, 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

Tetrofosmina in 12 other countries

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

All tetrofosmina products

Authorised across Europe · EMA

The same active substance is authorised in 21 EEA countries. Names it is sold under:

  • Austria · Myoview, Tetrofosmin Rotop
  • Belgium · Myoview, Tetrofosmin Rotop
  • Bulgaria · Майовю
  • Cyprus · Myoview
  • Czechia · Myoview
  • Germany · Myoview, Tetrofosmin Rotop
  • Denmark · Myoview
  • Finland · Myoview, Tetrofosmin Rotop
  • France · Myoview
  • United Kingdom (Northern Ireland) · Myoview, Tetrofosmin Rotop
  • Greece · Myoview, Tetrofosmin Rotop
  • Hungary · Myoview
  • Ireland · Myoview
  • Italy · Myoview
  • Luxembourg · Myoview
  • Malta · Myoview
  • Netherlands · Myoview, Tetrofosmine Rotop
  • Norway · Myoview
  • Portugal · Myoview, Tetrofosmina Rotop
  • Sweden · Myoview, Tetrofosmin Rotop
  • Slovakia · Myoview

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 AEMPS CIMA (Spain). 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/44bfd519-689c-4f16-aa48-f4d6721d2d92
GET /v1/drugs/44bfd519-689c-4f16-aa48-f4d6721d2d92?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.

{
  "cpresc": "Uso Hospitalario",
  "estado": "{\"aut\":1549234800000}",
  "nregistro": "83803",
  "substance": "tetrofosmina"
}

See everything about tetrofosmina.

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.