Iceland· IS-EU/1/01/189/001-003

Replagal

A agalsidase alfa product containing agalsidasum alfa inn, registered in Iceland by Takeda Pharmaceuticals International AG Ireland Branch. The same ATC class is registered in 13 of our 19 countries.

ATC A16AB03

Checked against Icelandic Medicines Agency (Iceland) on

Informational only — not a medical device.

SOURCE REGISTER · ISIcelandic Medicines Agency (Iceland)normalisedReplagalATCA16AB03REGISTER NO.IS-EU/1/01/189/001-003PACKS LISTED1CHECKEDSeptember 29, 2026

Where it is registered

Agalsidase alfa is registered in 13 of 19 countries.

Countries holding a registration under ATC A16AB03 (agalsidase alfa), each read from that country’s own register.

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

Agalsidase alfa · ATC A16AB03

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
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
Agalsidasum alfa INN
Manufacturer
Takeda Pharmaceuticals International AG Ireland Branch
Country
Iceland (IS)
ATC code
A16AB03
ATC class
Agalsidase alfa
Defined daily dose
1 mg, P
Reimbursed
Not published by this register
Source register
Icelandic Medicines Agency (Iceland)
Last checked
September 29, 2026

Packs & prices · 1

1 priced
  • ean
    007601
    3,5 ml x1 hgl
    ISK 279858

Regulatory notes

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

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/22b77f55-2a44-45a5-a1b5-ed4952efe602
GET /v1/drugs/22b77f55-2a44-45a5-a1b5-ed4952efe602?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": "Innrennslisþykkni, lausn",
  "source": "lyfjastofnun",
  "atc_raw": "A16AB03",
  "marketed": true,
  "strength": "1 mg/ml",
  "ma_number": "EU/1/01/189/001-003",
  "substance": "Agalsidasum alfa INN",
  "other_info": "Ávísun lyfsins er bundin við sérfræðinga í hjartasjúkdómum og sérfræðinga í nýrnasjúkdómum.\r\nMarkaðssetning á Íslandi er háð því að Lyfjastofnun hafi staðfest að sérstök skilyrði er varða öryggi og verkun við notkun lyfsins séu uppfyllt.",
  "legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
  "ma_issued_serial": "37161"
}

See everything about agalsidase alfa.

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.