# Gozellix

NDC: 84552-500
Generic name: GOZETOTIDE
Labeler / Manufacturer: Telix Innovations SA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20250320

FDA application: NDA219592

## 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:"84552-500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84552-500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=abeab169-e38e-433a-b8a9-f1dab31518c8