EMPLICITI

UNIISPLATC L01FX08

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerE.R. Squibb & Sons, L.L.C.

CountryUS (United States)

ATC codeL01FX08

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0003229111
1 VIAL, SINGLE-USE in 1 CARTON (0003-2291-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

1351PE5UGS

ELOTUZUMAB

RxCUI 1726104

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1351PE5UGS",
    "rxcui": "1726104",
    "inchikey": null,
    "display_name": "ELOTUZUMAB",
    "substance_type": "protein",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "80686b7e-f6f4-4154-b5c0-c846425e2d91": {
      "match": "brand_token",
      "title": "EMPLICITI (ELOTUZUMAB) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]",
      "spl_version": "13",
      "published_date": "2024-06-28"
    }
  },
  "productid": "0003-2291_8441efc2-338a-4d1d-8fa1-9b9863a49ffd",
  "productndc": "0003-2291",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ELOTUZUMAB",
  "proprietary_name": "EMPLICITI",
  "active_ingred_unit": "mg/1",
  "application_number": "BLA761035",
  "marketing_category": "BLA",
  "nonproprietary_name": "elotuzumab",
  "start_marketing_date": "20151130",
  "active_numerator_strength": "300"
}

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