Poland· PL-100492147
Elrexfio
A other monoclonal antibodies and antibody drug conjugates product containing elranatamabum, registered in Poland by Pfizer Europe MA EEIG. The same ATC class is registered in 5 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Elranatamabum is registered in 5 of 19 countries.
Countries holding a registration under ATC L01FX (other monoclonal antibodies and antibody drug conjugates), 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
Elranatamabum · ATC L01FX
5 / 19 countries
- Finlandprice
- Icelandprice
- Netherlands
- Polandprice
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Elranatamabum
- Manufacturer
- Pfizer Europe MA EEIG
- Country
- Poland (PL)
- ATC code
- L01FX
- ATC class
- Other monoclonal antibodies and antibody drug conjugates
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05415062116289
- gtin05415062116272
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Elranatamabum in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumElrexfio 40 mg/mlPfizer Europe MA
- SwitzerlandElrexfio
- CzechiaELREXFIOPfizer Europe MA EEIG, Bruxelles
- SpainELREXFIO 40 MG/ML SOLUCION INYECTABLEPfizer Europe Ma Eeig
- IcelandElrexfioPfizer Europe MA EEIG*
- NorwayElrexfioPfizer Europe MA EEIG
- SwedenELREXFIO 40 mg/ml Injektionsvätska, lösningPfizer Europe MA EEIG
- United StatesElrexfioU.S. Pharmaceuticals
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Elrexfio
- Liechtenstein · Elrexfio
- Norway · Elrexfio
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/28248d53-e9e4-4ec2-bc70-d4c1ac690c7a GET /v1/drugs/28248d53-e9e4-4ec2-bc70-d4c1ac690c7a?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": "40 mg/ml",
"packaging": "05415062116289 ¦ Rpz ¦ EU/1/23/1770/001 ¦ 152791\n1 fiol. 1,1 ml\n05415062116272 ¦ Rpz ¦ EU/1/23/1770/002 ¦ 152792\n1 fiol. 1,9 ml",
"substance": "Elranatamabum 40 mg/ml",
"common_name": "Elranatamabum",
"pl_product_id": "100492147",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about elranatamabum.
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.