# Norditropin

NDC: 0169-7705
Generic name: somatropin
Labeler / Manufacturer: Novo Nordisk
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20060102

FDA application: BLA021148

## Active ingredients

- SOMATROPIN: 10 mg/1.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0169-7705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0169-7705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1058e17c-9261-459c-a3e6-fae38d196c14