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Sweden· SE-20181031000062

Aklief 50 mikrogram/g Kräm

A medicinal product containing trifarotene, registered in Sweden by Galderma Nordic AB.

Checked against Swedish Medical Products Agency (Sweden) on

Informational only — not a medical device.

SOURCE REGISTER · SESwedish Medical Products Agency (Sweden)normalisedAklief 50 mikrogram/g KrämATC—REGISTER NO.SE-20181031000062PACKS LISTED1CHECKEDOctober 1, 2026

The record

At a glance

Swedish Medical Products Agency (Sweden)
Active substance
Trifarotene
Manufacturer
Galderma Nordic 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
    20181031000062

Regulatory notes

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

Same medicine, other countries

Trifarotene in 15 other countries

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

All trifarotene products

Authorised across Europe · EMA

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

  • Belgium · Aklief
  • Bulgaria · Аклиеф
  • Cyprus · Selgamis
  • Czechia · Aklief
  • Germany · Selgamis
  • Denmark · Aklief
  • Estonia · Aklief
  • Spain · Aklief
  • Finland · Aklief
  • France · Aklief
  • United Kingdom (Northern Ireland) · Aklief
  • Greece · Selgamis
  • Croatia · Aklief
  • Hungary · Aklief
  • Ireland · Aklief
  • Iceland · Aklief
  • Italy · Selgamis
  • Lithuania · Aklief
  • Luxembourg · Aklief
  • Latvia · Aklief
  • Malta · Aklief
  • Netherlands · Aklief
  • Norway · Aklief
  • Poland · Aklief
  • Portugal · Aklief
  • Romania · Aklief
  • Slovakia · Aklief

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/409dcdcd-736f-47f2-9942-b6871f4c8cd8
GET /v1/drugs/409dcdcd-736f-47f2-9942-b6871f4c8cd8?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",
    "PL",
    "sPAR",
    "PAR"
  ],
  "se_npl_id": "20181031000062",
  "product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=20181031000062",
  "product_doc_link": "https://docetp.mpa.se/LMF/Aklief%20cream%20ENG%20SmPC_09001bee80a46124.pdf"
}

See everything about trifarotene.

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.