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Netherlands· NL-648e5db32147

Elfabrio 2 mg/ml concentraat voor oplossing voor infusie

A pegunigalsidase alfa product containing pegunigalsidase alfa, registered in Netherlands by Chiesi Farmaceutici S.p.A.. The same ATC class is registered in 12 of our 19 countries.

ATC A16AB20

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedElfabrio 2 mg/ml concentraat voor opl…ATCA16AB20REGISTER NO.NL-648e5db32147PACKS LISTED1CHECKEDSeptember 29, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about pegunigalsidase alfaAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Pegunigalsidase alfa is registered in 12 of 19 countries.

Countries holding a registration under ATC A16AB20 (pegunigalsidase alfa), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 8 of them publish a price we can compare per daily dose
Search pegunigalsidase alfa products by name

Pegunigalsidase alfa · ATC A16AB20

12 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • 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

CBG-MEB (Netherlands)
Active substance
PEGUNIGALSIDASE ALFA
Manufacturer
Chiesi Farmaceutici S.p.A.
Country
Netherlands (NL)
ATC code
A16AB20
ATC class
Pegunigalsidase alfa
Defined daily dose
5 mg, P
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/23/1724

Regulatory notes

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

Same medicine, other countries

Pegunigalsidase alfa in 12 other countries

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

All pegunigalsidase alfa products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Elfabrio
  • Liechtenstein · Elfabrio
  • Norway · Elfabrio

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 CBG-MEB (Netherlands). 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/a9168d13-72cb-4ea6-aba2-05e79d75c715
GET /v1/drugs/a9168d13-72cb-4ea6-aba2-05e79d75c715?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": "Concentraat voor oplossing voor infusie",
  "route": "Intraveneus gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/elfabrio-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Pegunigalsidase alfa",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp129580",
  "excipients": [
    "CITROENZUUR 0-WATER (E 330)",
    "NATRIUMCHLORIDE",
    "STIKSTOF (HEAD SPACE) (E 941)",
    "TRINATRIUMCITRAAT 2-WATER (E 331)",
    "WATER VOOR INJECTIE"
  ],
  "substances": [
    "PEGUNIGALSIDASE ALFA"
  ],
  "leaflet_url": null,
  "authorised_at": "2023/05/04",
  "procedure_number": "EMEA/H/C/005618",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/23/1724",
  "additional_monitoring": "Y"
}
API referenceMCP serverPlans

See everything about pegunigalsidase 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.

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