United States · FDA National Drug Code directory
ZYFLO
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
- 10122-901_d49e40c7-0635-4220-8b0a-c5068116ee17
- Product NDC
- 10122-901
- Form
- TABLET
- Composition / generic term
- zileuton
- Labeler
- Chiesi USA, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19961206 / 20271130
Source-listed ingredients
- ZILEUTON — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (10122-901-12) · 10122-901-12
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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