Poland· PL-100377641

Sialanar

A glycopyrronium bromid product containing glycopyrronii bromidum, registered in Poland by Proveca Pharma Limited. The same ATC class is registered in 12 of our 19 countries.

ATC A03AB02

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedSialanarATCA03AB02REGISTER NO.PL-100377641PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Glycopyrronium bromid is registered in 12 of 19 countries.

Countries holding a registration under ATC A03AB02 (glycopyrronium bromid), each read from that country’s own register.

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

Glycopyrronium bromid · ATC A03AB02

12 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • Norwayprice
  • Polandprice
  • 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

URPL (Poland)
Active substance
Glycopyrronii bromidum
Manufacturer
Proveca Pharma Limited
Country
Poland (PL)
ATC code
A03AB02
ATC class
Glycopyrronium bromid
Defined daily dose
3 mg, O
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05060506950136
  • gtin
    04150139469318

Regulatory notes

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

Same medicine, other countries

Glycopyrronium bromid in 11 other countries

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

All glycopyrronium bromid products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • Austria · Rybrila
  • Germany · Rybrila
  • Spain · Axhidrox
  • Sweden · Glycopyrronium Cantabria

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/af68f88c-aa8c-4b2f-b00f-1f28aa2a47ae
GET /v1/drugs/af68f88c-aa8c-4b2f-b00f-1f28aa2a47ae?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": "Roztwór doustny",
  "source": "urpl",
  "strength": "320 mcg/ml",
  "packaging": "05060506950136 ¦ Rpz ¦ EU/1/16/1135/001 ¦ 117912\n1 butelka 250 ml ¦ 1 strzyk. 8 ml\n¦ UR/Z/4c/184/22 - 04150139469318 ¦ UR/Z/4c/083/23 - 04150139469318 ¦ UR/Z/4c/169/22 - 04150139469318\nRpz ¦ EU/1/16/1135/002 ¦ 148309\n1 butelka 60 ml ¦ 1 strzyk. 8 ml",
  "substance": "Glycopyrronii bromidum 320 mcg/ml",
  "common_name": "Glycopyrronii bromidum",
  "pl_product_id": "100377641",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about glycopyrronium bromid.

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.