Switzerland· 69910001
Blenrep 70 mg, Pulver für ein Konzentrat zur Herstellung einer Infusionslösung
A belantamab mafodotin product containing belantamabum mafodotinum, registered in Switzerland by GlaxoSmithKline AG and dispensed under Swissmedic category A. The same ATC class is registered in 12 of our 19 countries.
Checked against Swissmedic (Switzerland) 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: Switzerland, from Swissmedic (Switzerland)
- 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
Swissmedic (Switzerland)- Active substance
- belantamabum mafodotinum
- Manufacturer
- GlaxoSmithKline AG
- Country
- Switzerland (CH)
- ATC code
- L01FX15
- ATC class
- Belantamab mafodotin
- Defined daily dose
- 8.3 mg, P
- Swissmedic category
- A
- Reimbursed
- No
- Source register
- Swissmedic (Switzerland)
- Last checked
- September 12, 2026
Packs & prices · 0
No packs listed by the register for this record.
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.
- BelgiumBlenrep 70 mgGlaxoSmithKline Trading Services
- CzechiaBLENREPGlaxoSmithKline Trading Services Limited, Dublin
- SpainBLENREP 70 MG POLVO PARA CONCENTRADO PARA SOLUCION PARA PERFUSIONGlaxosmithkline Trading Services Limited
- FinlandBLENREPGlaxosmithkline Trading Services Limited
- United KingdomBlenrep 70mg powder for concentrate for solution for infusion vialsGlaxoSmithKline UK Ltd
- IrelandBLENREP 70 mg powder for concentrate for solution for infusionGlaxoSmithKline Trading Services Limited
- IcelandBlenrepGlaxoSmithKline Trading Services Limited
- NorwayBlenrepGlaxoSmithKline Trading Services Limited
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 Swissmedic (Switzerland). 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/bb3a771b-1bef-4309-b959-ba1ff5921417 GET /v1/drugs/bb3a771b-1bef-4309-b959-ba1ff5921417?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.
{
"source": "swissmedic_auth",
"heilmittelcode": "Biotechnologika"
}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.