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Switzerland· 58224001

Naglazyme, Konzentrat zur Herstellung einer Infusionslösung

A galsulfase product containing galsulfasum, registered in Switzerland by DRAC AG and dispensed under Swissmedic category B, on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

Reimbursed in Switzerland (BAG SL)Cat B (Swissmedic)ATC A16AB08

Checked against Swissmedic (Switzerland) on

Informational only — not a medical device.

SOURCE REGISTER · CHSwissmedic (Switzerland)normalisedNaglazyme, Konzentrat zur Herstellung…ATCA16AB08REGISTER NO.58224001PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Galsulfase is registered in 14 of 19 countries.

Countries holding a registration under ATC A16AB08 (galsulfase), each read from that country’s own register.

  • This record: Switzerland, from Swissmedic (Switzerland)
  • 9 of them publish a price we can compare per daily dose

Galsulfase · ATC A16AB08

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • 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

Swissmedic (Switzerland)
Active substance
galsulfasum
Manufacturer
DRAC AG
Country
Switzerland (CH)
ATC code
A16AB08
ATC class
Galsulfase
Swissmedic category
B
Reimbursed
Yes
Source register
Swissmedic (Switzerland)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • gtin
    7680582240013
    Durchstf 5 ml
    CHF 1462.5

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 Swissmedic (Switzerland). 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/9ca194e1-6678-4808-af57-7b82011e218f
GET /v1/drugs/9ca194e1-6678-4808-af57-7b82011e218f?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.

{
  "unit": null,
  "strength": "galsulfasum 5 mg",
  "valid_from": "2025-10-01",
  "limitations": "[{\"description\":\"Verordnung nach Evaluation durch die klinische Expertengruppe der Swiss Group for Inborn Errors of Metabolism (SGIEM).<br>\\nJährliche Evaluation durch klinische Expertengruppe der SGIEM.<br>\\n<br>\",\"costApproval\":null,\"indication\":\"\",\"isNew\":false,\"limitationCode\":null,\"priceModel\":null,\"validFrom\":\"2025-10-01\"}]",
  "galenic_form": "Inf Konz 5 mg/5ml",
  "therapeutic_area": null,
  "sl_inclusion_date": "2025-10-01",
  "self_retention_pct": 10
}

See everything about galsulfase.

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.