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Prescription medicine

Elotuzumab Brand names: Empliciti

Elotuzumab (Empliciti) is a prescription medicine with an FDA approval on record since 2015. No generic is listed in FDA's NDC Directory.

  • No generic listed

Check it at the source: the elotuzumab FDA label on DailyMed (effective March 22, 2022, E.R. Squibb & Sons, L.L.C.); the BLA 761035 record on Drugs@FDA; every elotuzumab label on DailyMed.

Highlights of the record

FDA label of March 22, 2022; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

EMPLICITI is indicated in combination with lenalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one to three prior therapies.

Forms and strengths

  • 300 mg
  • 400 mg

Injection (powder) (lyophilized) for solution.

On the market

Earliest approval on file
November 30, 2015 Empliciti, Bristol Myers Squibb; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
5,137 through July 30, 2026

What is elotuzumab used for?

From the label: indications and usage

EMPLICITI is indicated in combination with lenalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one to three prior therapies.

EMPLICITI is indicated in combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least two prior therapies including lenalidomide and a proteasome inhibitor. EMPLICITI is a SLAMF7-directed immunostimulatory antibody indicated in

combination with lenalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one to three prior therapies. […]

Conditions named in the indications of elotuzumab's FDA labels, with every medicine labeled for each:

FDA pharmacologic class: SLAMF7-directed Immunostimulatory Antibody.

Source: FDA drug label (EMPLICITI), E.R. Squibb & Sons, L.L.C., effective March 22, 2022 (SPL set 80686b7e-f6f4-4154-b5c0-c846425e2d91), via openFDA; the full label on DailyMed

Is there a generic for elotuzumab (Empliciti)?

No generic elotuzumab is approved (Drugs@FDA, October 8, 2026).

  • 2015 earliest approval on file

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What does the elotuzumab label say about other medicines?

The elotuzumab label names 4 other medicines in its interaction, contraindication or warning sections. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
Acetaminophenwarnings and precautionsAdminister premedication consisting of dexamethasone, antihistamines (H1 and H2 blockers) and acetaminophen prior to EMPLICITI infusion [see Dosage and Administration (2.3) ].
Dexamethasonedrug interactionsDRUG INTERACTIONS 7.1 Drug Interactions For important drug interactions involving lenalidomide, pomalidomide and dexamethasone, refer to their respective prescribing information.
Lenalidomidedrug interactionsDRUG INTERACTIONS 7.1 Drug Interactions For important drug interactions involving lenalidomide, pomalidomide and dexamethasone, refer to their respective prescribing information.
Pomalidomidedrug interactionsDRUG INTERACTIONS 7.1 Drug Interactions For important drug interactions involving lenalidomide, pomalidomide and dexamethasone, refer to their respective prescribing information.

Check elotuzumab against other medicines

Source: FDA drug label (EMPLICITI), E.R. Squibb & Sons, L.L.C., effective March 22, 2022 (SPL set 80686b7e-f6f4-4154-b5c0-c846425e2d91), via openFDA; the full label on DailyMed

What do FAERS reports show for elotuzumab?

The FDA Adverse Event Reporting System holds 5,137 reports that list elotuzumab among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 918 are coded as a death and 2,010 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

Reports received each year

The most reported reactions

  • Plasma Cell Myeloma564
  • Pneumonia (named in the label)304
  • Death (an outcome recorded in the report)298
  • Malignant Neoplasm Progression254
  • Fatigue (named in the label)236
  • Diarrhoea (named in the label)231
  • Pyrexia (named in the label)221
  • Drug Ineffective (a use or a product term, not a reaction)203

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What else is labeled for the same conditions as elotuzumab?

36 other medicines are given the same way (intravenous) and in the same FDA class as elotuzumab or labeled mainly for the same use (leukemia, lymphoma and myeloma), the same class first. Leukemia, lymphoma and myeloma lists all 98 medicines labeled for it, by any route. The first 8 are below. They are listed as records, not as substitutes: whether one can replace another is a prescriber's decision.

MedicineShared indicationGeneric labelers (intravenous)Pharmacy costShortage
CyclophosphamideLeukemia, lymphoma and myeloma15 labelersn/aNo current entry
DoxorubicinLeukemia, lymphoma and myeloma16 labelersn/aNo current entry
BortezomibLeukemia, lymphoma and myeloma22 labelersn/aNo current entry
Arsenic trioxideLeukemia, lymphoma and myeloma16 labelersn/aA presentation being discontinued
BendamustineLeukemia, lymphoma and myeloma4 labelersn/aA presentation being discontinued
NelarabineLeukemia, lymphoma and myeloma12 labelersn/aNo current entry
IdarubicinLeukemia, lymphoma and myeloma2 labelersn/aNo current entry
ClofarabineLeukemia, lymphoma and myeloma9 labelersn/aNo current entry

Source: FDA drug labels (indications), NDC Directory, NADAC of October 7, 2026, FDA shortages (October 8, 2026)

What next?

Elotuzumab side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other