# ZAVZPRET

NDC: 0069-3500
Generic name: zavegepant
Labeler / Manufacturer: Pfizer Laboratories Div Pfizer Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20230601

FDA application: NDA216386

## Active ingredients

- ZAVEGEPANT HYDROCHLORIDE: 10 mg/.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0069-3500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0069-3500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c4a7aec-daef-4961-ba77-92f4b58be780
