Poland· PL-100474751

Nexviadyme

A avalglucosidase alfa product containing avalglucosidasum alfa, registered in Poland by Sanofi B.V.. The same ATC class is registered in 14 of our 19 countries.

ATC A16AB22

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedNexviadymeATCA16AB22REGISTER NO.PL-100474751PACKS LISTED4CHECKEDSeptember 27, 2026

Where it is registered

Avalglucosidase alfa is registered in 14 of 19 countries.

Countries holding a registration under ATC A16AB22 (avalglucosidase alfa), each read from that country’s own register.

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

Avalglucosidase alfa · ATC A16AB22

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.

Price per daily dose

What a daily dose of avalglucosidase alfa costs, country by country.

Normalised to the WHO defined daily dose (0.1 g), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Avalglucosidase alfa · price per daily dose (0.1 g)

USD · FX 28 Sept 2026

  • CH Switzerland$1265.54
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

URPL (Poland)
Active substance
Avalglucosidasum alfa
Manufacturer
Sanofi B.V.
Country
Poland (PL)
ATC code
A16AB22
ATC class
Avalglucosidase alfa
Defined daily dose
0.1 g, P
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 4

  • gtin
    05909991472498
  • gtin
    05909991472467
  • gtin
    05909991472481
  • gtin
    05909991472474

Regulatory notes

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

Same medicine, other countries

Avalglucosidase alfa in 15 other countries

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

All avalglucosidase alfa products

Authorised across Europe · EMA

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

  • Iceland · Nexviadyme
  • Liechtenstein · Nexviadyme
  • Norway · Nexviadyme

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 URPL (Poland). 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/99ae874e-d545-4593-88ad-c16304e9249a
GET /v1/drugs/99ae874e-d545-4593-88ad-c16304e9249a?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": "Proszek do przygotowania koncentratu do sporządzania roztworu do infuzji",
  "source": "urpl",
  "strength": "100 mg",
  "packaging": "05909991472498 ¦ Rpz ¦ EU/1/21/1579/003 ¦ 142947\n10 fiol. 100 mg proszku\n05909991472467 ¦ Rpz ¦ EU/1/21/1579/002 ¦ 142948\n5 fiol. 100 mg proszku\n05909991472481 ¦ Rpz ¦ EU/1/21/1579/004 ¦ 142949\n25 fiol. 100 mg proszku\n05909991472474 ¦ Rpz ¦ EU/1/21/1579/001 ¦ 142950\n1 fiol. 100 mg proszku",
  "substance": "Avalglucosidasum alfa 100 mg",
  "common_name": "Avalglucosidasum alfa",
  "pl_product_id": "100474751",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about avalglucosidase 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.