United States · FDA National Drug Code directory
ZONISADE
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
- 52652-8001_063fd04f-90bf-4b1f-99fe-4e2cdb5b1eea
- Product NDC
- 52652-8001
- Form
- SUSPENSION
- Composition / generic term
- ZONISAMIDE
- Labeler
- Azurity Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20220715
- Source listing expiry
- 20261231
Source-listed ingredients
- ZONISAMIDE — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (52652-8001-1) / 150 mL in 1 BOTTLE · 52652-8001-1
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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