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United States· US:0003-4522_8441efc2-338a-4d1d-8fa1-9b9863a49ffd

EMPLICITI

A elotuzumab product containing elotuzumab, registered in United States by E.R. Squibb & Sons, L.L.C.. The same ATC class is registered in 11 of our 19 countries.

ATC L01FX08US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedEMPLICITIATCL01FX08REGISTER NO.US:0003-4522_8441efc2…PACKS LISTED2CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about elotuzumabAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

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: United States, from FDA National Drug Code directory (United States)
  • 8 of them publish a price we can compare per daily dose
Search elotuzumab products by name

Elotuzumab · ATC L01FX08

11 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • 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 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
Open the full comparison — free accountDrug prices for market access

Elotuzumab · price per daily dose (50 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$222.01
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ELOTUZUMAB
Manufacturer
E.R. Squibb & Sons, L.L.C.
Country
United States (US)
ATC code
L01FX08
ATC class
Elotuzumab
Defined daily dose
50 mg, P
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    0003452211
    1 VIAL, SINGLE-USE in 1 CARTON (0003-4522-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE
  • ndc11
    0003-4522-11

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
Check elotuzumab against other medicinesHow interaction checks work

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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

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.

All elotuzumab products

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 FDA National Drug Code directory (United States). 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/22a6cc42-e2ab-4fcd-91ea-58d977e24618
GET /v1/drugs/22a6cc42-e2ab-4fcd-91ea-58d977e24618?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.

{
  "route": "INTRAVENOUS",
  "source": "ndc",
  "strength": "400",
  "substance": "ELOTUZUMAB",
  "productndc": "0003-4522",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "BLA761035",
  "marketing_category": "BLA"
}
API referenceMCP serverPlans

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.

Try it freeOpen in the console