Poland· PL-100334324

Viekirax

A ombitasvir, paritaprevir and ritonavir product containing ombitasvirum + paritaprevirum + ritonavirum, registered in Poland by AbbVie Deutschland GmbH & Co. KG. The same ATC class is registered in 6 of our 19 countries.

ATC J05AP53

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedViekiraxATCJ05AP53REGISTER NO.PL-100334324PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Ombitasvir, paritaprevir and ritonavir is registered in 6 of 19 countries.

Countries holding a registration under ATC J05AP53 (ombitasvir, paritaprevir and ritonavir), 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

Ombitasvir, paritaprevir and ritonavir · ATC J05AP53

6 / 19 countries

  • Belgiumprice
  • Denmark
  • Finlandprice
  • Polandprice
  • Spainprice
  • United Kingdom
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
Ombitasvirum + Paritaprevirum + Ritonavirum
Manufacturer
AbbVie Deutschland GmbH & Co. KG
Country
Poland (PL)
ATC code
J05AP53
ATC class
Ombitasvir, paritaprevir and ritonavir
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    08054083006888

Regulatory notes

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

Same medicine, other countries

Ombitasvir, paritaprevir and ritonavir in 3 other countries

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

All ombitasvir, paritaprevir and ritonavir products

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/ddef9012-ada6-4568-935f-9e6fa40980cc
GET /v1/drugs/ddef9012-ada6-4568-935f-9e6fa40980cc?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": "Tabletki powlekane",
  "source": "urpl",
  "strength": "12,5 mg + 75 mg + 50 mg",
  "packaging": "08054083006888 ¦ Rpz ¦ EU/1/14/982/001 ¦ 106215\n56 tabl.",
  "substance": "Ombitasvirum 12.5 mg + Paritaprevirum 75 mg + Ritonavirum 50 mg",
  "common_name": "Ombitasvirum + Paritaprevirum + Ritonavirum",
  "pl_product_id": "100334324",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": "2024-09-25"
}

See everything about ombitasvir, paritaprevir and ritonavir.

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.