# HUMATROPE

NDC: 0002-8148
Generic name: Somatropin
Labeler / Manufacturer: Eli Lilly and Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: KIT
Routes: INTRAMUSCULAR, SUBCUTANEOUS
Marketing started: 20060127

FDA application: BLA019640

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-8148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-8148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a774e1ae-3997-49ee-8b0e-99a2b315d409