Poland· PL-100533647

Rybrevant

A amivantamab product containing amivantamabum, registered in Poland by Janssen-Cilag International N.V.. The same ATC class is registered in 15 of our 19 countries.

ATC L01FX18

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedRybrevantATCL01FX18REGISTER NO.PL-100533647PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Amivantamab is registered in 15 of 19 countries.

Countries holding a registration under ATC L01FX18 (amivantamab), each read from that country’s own register.

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

Amivantamab · ATC L01FX18

15 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Japan
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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.

Price per daily dose

What a daily dose of amivantamab costs, country by country.

Normalised to the WHO defined daily dose (75 mg), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Amivantamab · price per daily dose (75 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$335.64
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

URPL (Poland)
Active substance
Amivantamabum
Manufacturer
Janssen-Cilag International N.V.
Country
Poland (PL)
ATC code
L01FX18
ATC class
Amivantamab
Defined daily dose
75 mg, P
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05413868126136
  • gtin
    04150197340932

Regulatory notes

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

Same medicine, other countries

Amivantamab in 15 other countries

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

All amivantamab products

Authorised across Europe · EMA

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

  • Iceland · Rybrevant
  • Liechtenstein · Rybrevant
  • Norway · Rybrevant

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/2765df9a-5634-49e3-9393-750a67d3b81f
GET /v1/drugs/2765df9a-5634-49e3-9393-750a67d3b81f?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": "Roztwór do wstrzykiwań",
  "source": "urpl",
  "strength": "3520 mg",
  "packaging": "05413868126136 ¦ Rpz ¦ EU/1/21/1594/005 ¦ 165947\n1 fiol. 22 ml\n¦ UR/Z/4c/056/26 - 04150197340932",
  "substance": "Amivantamabum 3520 mg",
  "common_name": "Amivantamabum",
  "pl_product_id": "100533647",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about amivantamab.

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.