# EMPLICITI

NDC: 0003-4522
Generic name: elotuzumab
Labeler / Manufacturer: E.R. Squibb & Sons, L.L.C.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20151130

FDA application: BLA761035

## Active ingredients

- ELOTUZUMAB: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0003-4522"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0003-4522
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80686b7e-f6f4-4154-b5c0-c846425e2d91