Iceland· IS-EU/1/22/1652/001-002

Filsuvez

A birkenrinde product containing birch bark extract, registered in Iceland by Chiesi Farmaceutici S.p.A.*. The same ATC class is registered in 10 of our 19 countries.

ATC D03AX13

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedFilsuvezATCD03AX13REGISTER NO.IS-EU/1/22/1652/001-0…PACKS LISTED0CHECKEDSeptember 29, 2026

Where it is registered

Birkenrinde is registered in 10 of 19 countries.

Countries holding a registration under ATC D03AX13 (birkenrinde), each read from that country’s own register.

  • This record: Iceland, from Icelandic Medicines Agency (Iceland)
  • 7 of them publish a price we can compare per daily dose

Birkenrinde · ATC D03AX13

10 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
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

Icelandic Medicines Agency (Iceland)
Active substance
Birch bark extract
Manufacturer
Chiesi Farmaceutici S.p.A.*
Country
Iceland (IS)
ATC code
D03AX13
ATC class
Birkenrinde
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 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

Birkenrinde in 2 other countries

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

All birkenrinde products

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of Icelandic Medicines Agency (Iceland). 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/fba44a33-9256-4131-8def-0b314472b30a
GET /v1/drugs/fba44a33-9256-4131-8def-0b314472b30a?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.

{
  "form": "Hlaup",
  "source": "lyfjastofnun",
  "atc_raw": "D03AX13",
  "marketed": false,
  "strength": "100 mg/g",
  "ma_number": "EU/1/22/1652/001-002",
  "substance": "Birch bark extract",
  "other_info": null,
  "legal_status": "(R) Lyfseðilsskylt",
  "ma_issued_serial": "44733"
}

See everything about birkenrinde.

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.