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Germany· DE-A57-e585d2b387c28c54

Selgamis

A trifarotene product containing trifarotene, registered in Germany by Galderma Laboratorium Gmbh. The same ATC class is registered in 15 of our 19 countries.

ATC D10AD06

Checked against EMA Article 57 (European Union) on

Informational only — not a medical device.

SOURCE REGISTER · DEEMA Article 57 (European Union)normalisedSelgamisATCD10AD06REGISTER NO.DE-A57-e585d2b387c28c…PACKS LISTED0CHECKEDSeptember 30, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about trifaroteneAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Trifarotene is registered in 15 of 19 countries.

Countries holding a registration under ATC D10AD06 (trifarotene), each read from that country’s own register.

  • This record: Germany, from EMA Article 57 (European Union)
  • 9 of them publish a price we can compare per daily dose
Search trifarotene products by name

Trifarotene · ATC D10AD06

15 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Germany
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

EMA Article 57 (European Union)
Active substance
Trifarotene
Manufacturer
Galderma Laboratorium Gmbh
Country
Germany (DE)
ATC code
D10AD06
ATC class
Trifarotene
Defined daily dose
50 mcg, T
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.

Interactions

9 interactions on record for trifarotene.

Graded by severity as the source publishes them — 1 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan
Check trifarotene against other medicinesHow interaction checks work

Trifarotene · interactions on record

9 records

  • 1 severe
  • 8 moderate

Most severe, free to view

  • Aminolevulinic acidL01XD04severe
  • Salicylic acidD01AE12moderate
  • IsotretinoinD10AD04moderate
  • Benzoyl peroxideD10AE01moderate
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

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
  • 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
  • Sweden · 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 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/11a26e5b-a391-4ede-b0fe-1c47bb9c34ba
GET /v1/drugs/11a26e5b-a391-4ede-b0fe-1c47bb9c34ba?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": "Cutaneous Use",
  "source": "ema_art57_de",
  "ma_number": null,
  "substance": "Trifarotene",
  "atc_from_source": null,
  "authorisation_country": "Germany"
}
API referenceMCP serverPlans

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.

Try it freeOpen in the console