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Sweden· SE-19900302000037

TechneScan DTPA 20,8 mg Beredningssats för radioaktivt läkemedel

A medicinal product containing pentetic acid, registered in Sweden by Curium Netherlands B.V..

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedTechneScan DTPA 20,8 mg Beredningssat…ATC—REGISTER NO.SE-19900302000037PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Pentetic Acid
Manufacturer
Curium Netherlands B.V.
Country
Sweden (SE)
ATC code
—
Reimbursed
Not published by this register
Source register
Swedish Medical Products Agency (Sweden)
Last checked
October 1, 2026

Packs & prices · 1

  • se_varunummer
    19900302000037

Regulatory notes

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

Same medicine, other countries

Pentetic acid in 9 other countries

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

All pentetic acid products

Authorised across Europe · EMA

The same active substance is authorised in 16 EEA countries. Names it is sold under:

  • Austria · Technescan Dtpa
  • Belgium · Technescan Dtpa
  • Czechia · Technescan Dtpa
  • Germany · Technescan Dtpa
  • Denmark · Technescan Dtpa
  • Spain · Dtpa Technescan
  • Finland · Technescan Dtpa
  • France · Technescan Dtpa
  • United Kingdom (Northern Ireland) · Technescan Dtpa
  • Greece · Technescan Dtpa
  • Hungary · Dtpa Izotóp Intézet, Renon
  • Ireland · Technescan Dtpa
  • Italy · Technescan Dtpa
  • Netherlands · Technescan Dtpa
  • Portugal · Technescan Dtpa
  • Slovakia · Technescan Dtpa

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 Swedish Medical Products Agency (Sweden). 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/8ccd2d36-0dbe-42c7-abb6-19c5d91e260a
GET /v1/drugs/8ccd2d36-0dbe-42c7-abb6-19c5d91e260a?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.

{
  "source": "lakemedelsverket",
  "doc_types": [
    "SmPC"
  ],
  "se_npl_id": "19900302000037",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19900302000037",
  "product_doc_link": "https://docetp.mpa.se/LMF/TechneScan%20DTPA%20kit%20for%20radiopharmaceutical%20preparation%20SmPC_09001bee807a6e49.pdf"
}

See everything about pentetic acid.

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.