# SOMAVERT

NDC: 0009-7200
Generic name: pegvisomant
Labeler / Manufacturer: Pharmacia & Upjohn Company LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: KIT
Routes: —
Marketing started: 20161001

FDA application: BLA021106

## 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:"0009-7200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0009-7200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3cbb485b-6df1-49ce-8747-592b395b1988