Poland· PL-100526001

Zurzuvae

A other antidepressants product containing zuranolonum, registered in Poland by Biogen Netherlands B.V.. The same ATC class is registered in 4 of our 19 countries.

ATC N06AX

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedZurzuvaeATCN06AXREGISTER NO.PL-100526001PACKS LISTED0CHECKEDSeptember 27, 2026

Where it is registered

Zuranolonum is registered in 4 of 19 countries.

Countries holding a registration under ATC N06AX (other antidepressants), each read from that country’s own register.

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

Zuranolonum · ATC N06AX

4 / 19 countries

  • Belgiumprice
  • Polandprice
  • Switzerlandprice
  • 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
Zuranolonum
Manufacturer
Biogen Netherlands B.V.
Country
Poland (PL)
ATC code
N06AX
ATC class
Other antidepressants
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 0

No packs listed by the register for this record.

Regulatory notes

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

Same medicine, other countries

Zuranolonum in 8 other countries

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

All zuranolonum products

Authorised across Europe · EMA

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

  • Iceland · Zurzuvae
  • Liechtenstein · Zurzuvae
  • Norway · Zurzuvae

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/ce16ee0d-eb21-4a29-8bfc-97f6c733c163
GET /v1/drugs/ce16ee0d-eb21-4a29-8bfc-97f6c733c163?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": "Kapsułki twarde",
  "source": "urpl",
  "strength": "20 mg",
  "packaging": "Rp ¦ EU/1/25/1977/001 ¦ 164017\n14 kaps.\nRp ¦ EU/1/25/1977/002 ¦ 164018\n28 kaps. w butelce\nRp ¦ EU/1/25/1977/003 ¦ 164019\n28 kaps. w blistrze",
  "substance": "Zuranolonum 20 mg",
  "common_name": "Zuranolonum",
  "pl_product_id": "100526001",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about zuranolonum.

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.