# Humulin R U-500

NDC: 0002-8501
Generic name: Insulin human
Labeler / Manufacturer: Eli Lilly and Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 19940331

FDA application: BLA018780

## Active ingredients

- INSULIN HUMAN: 500 [iU]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-8501"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-8501
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b60e8dd0-1d48-4dc9-87fd-e14675255e8c