FDA NDC Directory · JSON-LD · Markdown

ZYFLO

NDC 10122-901 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namezileuton
Labeler / ManufacturerChiesi USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020471
Dosage form / routeTABLET · ORAL
Active ingredientsZILEUTON (600 mg/1)
Marketing started19961206
Marketing ended20271130
Package count1

External sources

Source: openFDA. Public-domain (CC0).