# ZAVZPRET

NDC: 63539-135
Generic name: zavegepant
Labeler / Manufacturer: U.S. Pharmaceuticals
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:"63539-135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63539-135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1191475f-e999-49f4-a805-93ad08596b1b