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NDC 0003-2291, elotuzumab, injection, powder, lyophilized, for solution, from E.R. Squibb & Sons, L.L.C..

Product NDC
0003-2291
Status
Listed
Labeler
E.R. Squibb & Sons, L.L.C.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA761035
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0003-2291 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ELOTUZUMAB300 mg/1

Pharmacologic classes

Antibodies, Monoclonal [CS]; SLAMF7-directed Antibody Interactions [MoA]; SLAMF7-directed Immunostimulatory Antibody [EPC]

Package NDCNDC-11Package
0003-2291-11000032291111 VIAL, SINGLE-USE in 1 CARTON (0003-2291-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/80686b7e-f6f4-4154-b5c0-c846425e2d91

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0003-2291

Use it

Look up 0003-2291 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0003-2291 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0003-2291. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.