United States · FDA National Drug Code directory
ZAVZPRET
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63539-135_3f4a6bba-ce03-463b-9167-65580312987f
- Product NDC
- 63539-135
- Form
- SPRAY
- Composition / generic term
- zavegepant
- Labeler
- U.S. Pharmaceuticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20230601
- Source listing expiry
- 20261231
Source-listed ingredients
- ZAVEGEPANT HYDROCHLORIDE — 10 mg/.1mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (63539-135-02) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (63539-135-01) / .1 mL in 1 VIAL, SINGLE-DOSE · 63539-135-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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