Poland· PL-100505915

Loqtorzi

A toripalimab product containing toripalimabum, registered in Poland by TMC Pharma (EU) Ltd.. The same ATC class is registered in 12 of our 19 countries.

ATC L01FF13

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedLoqtorziATCL01FF13REGISTER NO.PL-100505915PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Toripalimab is registered in 12 of 19 countries.

Countries holding a registration under ATC L01FF13 (toripalimab), each read from that country’s own register.

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

Toripalimab · ATC L01FF13

12 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • United Kingdom
  • 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
Toripalimabum
Manufacturer
TMC Pharma (EU) Ltd.
Country
Poland (PL)
ATC code
L01FF13
ATC class
Toripalimab
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 1

  • gtin
    04150199715806

Regulatory notes

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

Same medicine, other countries

Toripalimab in 12 other countries

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

All toripalimab products

Authorised across Europe · EMA

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

  • Iceland · Loqtorzi
  • Liechtenstein · Loqtorzi
  • Norway · Loqtorzi

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/cae27903-f1a7-43a4-b498-d9a86f379ad9
GET /v1/drugs/cae27903-f1a7-43a4-b498-d9a86f379ad9?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": "Koncentrat do sporządzania roztworu do infuzji",
  "source": "urpl",
  "strength": "240 mg",
  "packaging": "Rpz ¦ EU/1/24/1853/001 ¦ 158205\n1 fiol. 6 ml\n¦ UR/Z/4c/113/26 - 04150199715806",
  "substance": "Toripalimabum 240 mg",
  "common_name": "Toripalimabum",
  "pl_product_id": "100505915",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about toripalimab.

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.