Poland· PL-100366092
Empliciti
A elotuzumab product containing elotuzumabum, registered in Poland by Bristol-Myers Squibb Pharma EEIG. The same ATC class is registered in 11 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Elotuzumab is registered in 11 of 19 countries.
Countries holding a registration under ATC L01FX08 (elotuzumab), 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
Elotuzumab · ATC L01FX08
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
Price per daily dose
What a daily dose of elotuzumab costs, country by country.
Normalised to the WHO defined daily dose (50 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
Elotuzumab · price per daily dose (50 mg)
USD · FX 28 Sept 2026
- CH Switzerland$222.01
The record
At a glance
URPL (Poland)- Active substance
- Elotuzumabum
- Manufacturer
- Bristol-Myers Squibb Pharma EEIG
- Country
- Poland (PL)
- ATC code
- L01FX08
- ATC class
- Elotuzumab
- Defined daily dose
- 50 mg, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909991265649
- gtin08027950032181
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
169 interactions on record for elotuzumab.
Graded by severity as the source publishes them — 30 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
Elotuzumab · interactions on record
169 records
- 30 severe
- 139 moderate
Most severe, free to view
- MipomersenC10AX11severe
- LomitapideC10AX12severe
- CladribineL01BB04severe
- PexidartinibL01EX15severe
- 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
Elotuzumab in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumEmpliciti 300 mgBristol-Myers Squibb Pharma
- CzechiaEMPLICITIBristol-Myers Squibb Pharma EEIG, Dublin
- FinlandEmplicitiBristol-Myers Squibb Pharma EEIG
- United KingdomEmpliciti 300mg powder for concentrate for solution for infusion vialsBristol-Myers Squibb Pharmaceuticals Ltd
- IrelandEmpliciti 300 mg powder for concentrate for solution for infusion.Bristol-Myers Squibb Pharma EEIG
- IcelandEmplicitiBristol-Myers Squibb Pharma EEIG*
- NorwayEmplicitiBristol-Myers Squibb Pharma EEIG
- SwedenEmpliciti 300 mg Pulver till koncentrat till infusionsvätska, lösningBristol-Myers Squibb Pharma EEIG
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Empliciti
- Liechtenstein · Empliciti
- Norway · Empliciti
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/6c9978ab-cc6e-40df-8d5a-40f52d7293a7 GET /v1/drugs/6c9978ab-cc6e-40df-8d5a-40f52d7293a7?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": "300 mg",
"packaging": "05909991265649 ¦ Rpz ¦ Skasowane ¦ EU/1/16/1088/001 ¦ 114558\n1 fiol. proszku\n08027950032181 ¦ Rpz ¦ EU/1/16/1088/001 ¦ 137684\n1 fiol. 300 mg proszku\n¦ UR/Z/4c/005/21 - 08027950032181",
"substance": "Elotuzumabum 300 mg",
"common_name": "Elotuzumabum",
"pl_product_id": "100366092",
"pozwolenie_nr": null,
"auth_procedure": "CEN",
"authorisation_validity": null
}See everything about elotuzumab.
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.