Poland· PL-100522173
Blenrep
A belantamab mafodotin product containing belantamabum mafodotini, registered in Poland by GlaxoSmithKline Trading Services Limited. The same ATC class is registered in 12 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Belantamab mafodotin is registered in 12 of 19 countries.
Countries holding a registration under ATC L01FX15 (belantamab mafodotin), 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
Belantamab mafodotin · ATC L01FX15
12 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
URPL (Poland)- Active substance
- Belantamabum mafodotini
- Manufacturer
- GlaxoSmithKline Trading Services Limited
- Country
- Poland (PL)
- ATC code
- L01FX15
- ATC class
- Belantamab mafodotin
- Defined daily dose
- 8.3 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05901549673012
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
58 interactions on record for belantamab mafodotin.
Graded by severity as the source publishes them — 28 severe. Severity grades are free for everyone; mechanism and management come with Growth.
- Severity for every pair — free, no plan needed
- The source, licence and sync date on every record
- Mechanism and what to do for each pair — Growth plan
Belantamab mafodotin · interactions on record
58 records
- 28 severe
- 30 moderate
Most severe, free to view
- CladribineL01BB04severe
- Talimogene laherparepvecL01XL02severe
- Talimogen laherparepvecL01XX51severe
- LeflunomidL04AA13severe
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Belantamab mafodotin in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwedenBlenrep 100 mg Pulver till koncentrat till infusionsvätska, lösningGlaxoSmithKline (Ireland) Limited
- SpainBLENREP 100 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONGlaxosmithkline (Ireland) Limited
- FinlandBlenrepGlaxoSmithKline (Ireland) Limited
- United KingdomBlenrep 100mg powder for concentrate for solution for infusion vialsGlaxoSmithKline UK Ltd
- BelgiumBlenrep 100 mgGlaxoSmithKline Trading Services
- NorwayBlenrepGlaxoSmithKline Trading Services Limited
- SwitzerlandBlenrep 100 mg, Pulver für ein Konzentrat zur Herstellung einer InfusionslösungGlaxoSmithKline AG
- CzechiaBLENREPGlaxoSmithKline Trading Services Limited, Dublin
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Blenrep
- Liechtenstein · Blenrep
- Norway · Blenrep
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/1d2c527e-f8d8-49e3-aeb0-99fab0544e15 GET /v1/drugs/1d2c527e-f8d8-49e3-aeb0-99fab0544e15?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": "Proszek do sporządzania koncentratu roztworu do infuzji",
"source": "urpl",
"strength": "100 mg",
"packaging": "05901549673012 ¦ Rpz ¦ EU/1/25/1948/002 ¦ 163106\n1 fiol. 6 ml",
"substance": "Belantamabum mafodotini 100 mg",
"common_name": "Belantamabum mafodotini",
"pl_product_id": "100522173",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about belantamab mafodotin.
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.