# Humulin 70/30 KwikPen

NDC: 0002-8803
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: BLA019717

## Active ingredients

- INSULIN HUMAN: 100 [iU]/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-8803"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-8803
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e245e0c5-b2d6-418b-baa4-1c3324292885