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Ireland· IE-PA-EU/1/17/1213/001

Maviret 100 mg/40 mg film-coated tablets

A other antivirals product containing pibrentasvir + glecaprevir, registered in Ireland by AbbVie Deutschland GmbH & Co. KG. The same ATC class is registered in 4 of our 19 countries.

ATC J05AX

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedMaviret 100 mg/40 mg film-coated tabl…ATCJ05AXREGISTER NO.IE-PA-EU/1/17/1213/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Pibrentasvir + glecaprevir is registered in 4 of 19 countries.

Countries holding a registration under ATC J05AX (other antivirals), each read from that country’s own register.

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

Pibrentasvir + glecaprevir · ATC J05AX

4 / 19 countries

  • Canada
  • Ireland
  • Netherlands
  • 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

HPRA (Ireland)
Active substance
Pibrentasvir + Glecaprevir
Manufacturer
AbbVie Deutschland GmbH & Co. KG
Country
Ireland (IE)
ATC code
J05AX
ATC class
Other antivirals
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/17/1213/001

Regulatory notes

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

Same medicine, other countries

Pibrentasvir + glecaprevir in 13 other countries

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

All pibrentasvir + glecaprevir products

Authorised across Europe · EMA

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

  • United Kingdom (Northern Ireland) · Glecaprevir/Pibrentasvir Abbvie
  • Iceland · Maviret
  • Liechtenstein · Maviret
  • Norway · Maviret

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/cd340baa-09f9-434a-9e96-80509b2177bb
GET /v1/drugs/cd340baa-09f9-434a-9e96-80509b2177bb?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": [
    "J05AX"
  ],
  "strength": null,
  "pa_number": "EU/1/17/1213/001",
  "substances": [
    "Pibrentasvir",
    "Glecaprevir"
  ],
  "legal_basis": "Known active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "26/07/2017",
  "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 pibrentasvir + glecaprevir.

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.