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Ireland· IE-PA-EU/1/16/1138/003-004

Venclyxto 50 mg film-coated tablets

A other antineoplastic agents product containing venetoclax, registered in Ireland by AbbVie Deutschland GmbH & Co. KG. The same ATC class is registered in 5 of our 19 countries.

ATC L01X

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedVenclyxto 50 mg film-coated tabletsATCL01XREGISTER NO.IE-PA-EU/1/16/1138/00…PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Venetoclax is registered in 5 of 19 countries.

Countries holding a registration under ATC L01X (other antineoplastic agents), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 3 of them publish a price we can compare per daily dose

Venetoclax · ATC L01X

5 / 19 countries

  • Belgiumprice
  • Canada
  • Finlandprice
  • Ireland
  • Switzerlandprice
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

HPRA (Ireland)
Active substance
Venetoclax
Manufacturer
AbbVie Deutschland GmbH & Co. KG
Country
Ireland (IE)
ATC code
L01X
ATC class
OTHER ANTINEOPLASTIC AGENTS
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/16/1138/003-004

Regulatory notes

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

Same medicine, other countries

Venetoclax in 14 other countries

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

All venetoclax products

Authorised across Europe · EMA

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

  • United Kingdom (Northern Ireland) · Venclyxto
  • Iceland · Venclyxto
  • Liechtenstein · Venclyxto
  • Norway · Venclyxto

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 HPRA (Ireland). 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/ed5b270b-3ba6-450f-8cbf-5d66e30f1442
GET /v1/drugs/ed5b270b-3ba6-450f-8cbf-5d66e30f1442?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": "Film-coated tablet",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "L01X"
  ],
  "strength": null,
  "pa_number": "EU/1/16/1138/003-004",
  "substances": [
    "Venetoclax"
  ],
  "legal_basis": "Full application (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "05/12/2016",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about venetoclax.

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.