# Zileuton

NDC: 51407-741
Generic name: zileuton
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, MULTILAYER, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191216

FDA application: ANDA212670

## 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:"51407-741"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-741
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7573809-7741-04c9-e053-6294a90ab193