# Humulin N

NDC: 0002-8805
Generic name: Insulin human
Labeler / Manufacturer: Eli Lilly and Company
Product type: HUMAN OTC DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SUSPENSION
Routes: SUBCUTANEOUS
Marketing started: 20131107

FDA application: BLA018781

## Active ingredients

- INSULIN HUMAN: 100 [iU]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-8805"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-8805
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6edd793-440b-40c2-96b5-c16133b7a921