Finland· FI-REL-REL238

Nelex

A policresulen product containing policresulen, registered in Finland by Byk Gulden Lomberg Chemische Fabrik Gmbh. The same ATC class is registered in 4 of our 19 countries.

ATC G01AX03

Checked against Fimea (Finland) on

Informational only — not a medical device.

SOURCE REGISTER · FIFimea (Finland)normalisedNelexATCG01AX03REGISTER NO.FI-REL-REL238PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Policresulen is registered in 4 of 19 countries.

Countries holding a registration under ATC G01AX03 (policresulen), each read from that country’s own register.

  • This record: Finland, from Fimea (Finland)
  • 3 of them publish a price we can compare per daily dose

Policresulen · ATC G01AX03

4 / 19 countries

  • Finlandprice
  • Germany
  • Norwayprice
  • Polandprice
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

Fimea (Finland)
Active substance
Policresulen
Manufacturer
Byk Gulden Lomberg Chemische Fabrik Gmbh
Country
Finland (FI)
ATC code
G01AX03
ATC class
Policresulen
Defined daily dose
90 mg, V
Reimbursed
Not published by this register
Source register
Fimea (Finland)
Last checked
September 27, 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

Policresulen in 4 other countries

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

All policresulen products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Germany · Albothyl
  • Poland · Albothyl

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 Fimea (Finland). 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/9cab1b74-5619-4aa1-a2ee-3c3622c32d68
GET /v1/drugs/9cab1b74-5619-4aa1-a2ee-3c3622c32d68?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.

{
  "ddd": "90",
  "form": "emätinpuikko",
  "route": null,
  "ddd_unit": "mg",
  "strength": "90 mg",
  "atc_label": "polikresuleeni",
  "ma_number": "2082",
  "auth_status": "Myyntilupa peruuntunut",
  "eu_ma_number": null,
  "fimea_rel_id": "REL238",
  "authorised_at": "1965-08-18"
}

See everything about policresulen.

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.