# ZYFLO

NDC: 10122-901
Generic name: zileuton
Labeler / Manufacturer: Chiesi USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19961206
Marketing ended: 20271130
FDA application: NDA020471

## Active ingredients

- ZILEUTON: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10122-901"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10122-901
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aee65202-fddb-497f-9f11-17cc727cb157