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Sweden· SE-20080510000022

IRESSA 250 mg Filmdragerad tablett

A medicinal product containing gefitinib, registered in Sweden by AstraZeneca AB.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedIRESSA 250 mg Filmdragerad tablettATC—REGISTER NO.SE-20080510000022PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Gefitinib
Manufacturer
AstraZeneca AB
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
    20080510000022

Regulatory notes

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

Same medicine, other countries

Gefitinib in 15 other countries

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

All gefitinib products

Authorised across Europe · EMA

The same active substance is authorised in 27 EEA countries. Names it is sold under:

  • Austria · Gefitinib Accord
  • Belgium · Gefitinib Accord, Gefitinib Sandoz
  • Bulgaria · Фромпо
  • Cyprus · Refetib
  • Czechia · Gefitinib Accord
  • Germany · Gefitinib Accord, Gefitinib Genthon
  • Denmark · Gefitinib Accord, Gefitinib Stada
  • Estonia · Gefitinib Auxilia, Gefitinib Norameda
  • Spain · Gefitinib Efg Genthon, Gefitinib Eugia
  • Finland · Gefitinib Accord, Gefitinib Stada
  • France · Gefitinib Arrow, Gefitinib Biogaran
  • United Kingdom (Northern Ireland) · Gefitinib Accord, Gefitinib Eugia (Uk)
  • Greece · Gefitinib Faran, Gefitinib Genepharm
  • Croatia · Gefitinib Pliva, Gefitinib Sandoz
  • Hungary · Gefitinib Genepharm, Gefitinib Onkogen
  • Iceland · Gefitinib Stada, Gefitinib Wh
  • Italy · Gefitinib Medac
  • Liechtenstein · Iressa
  • Lithuania · Gefitinib Norameda
  • Latvia · Gefitinib Norameda
  • Malta · Gefitinib Eugia, Gefitinib Genthon
  • Netherlands · Gefitinib Eugia, Gefitinib Genthon
  • Norway · Gefitinib Stada, Iressa
  • Poland · Gefitinib Accord, Gefitinib Genthon
  • Portugal · Gefitinib Accord, Gefitinib Eugia
  • Romania · Gefitinib Accord, Gefitinib Polisano
  • Slovenia · Phrompo

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/a9bebf3e-f534-45d9-a6f8-1d551c891703
GET /v1/drugs/a9bebf3e-f534-45d9-a6f8-1d551c891703?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": [
    "EPAR",
    "EMA"
  ],
  "se_npl_id": "20080510000022",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20080510000022",
  "product_doc_link": "https://www.ema.europa.eu/sv/documents/product-information/iressa-epar-product-information_sv.pdf"
}

See everything about gefitinib.

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.