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Zileuton

NDC 51407-741 · HUMAN PRESCRIPTION DRUG · TABLET, MULTILAYER, EXTENDED RELEASE

Generic namezileuton
Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212670
Dosage form / routeTABLET, MULTILAYER, EXTENDED RELEASE · ORAL
Active ingredientsZILEUTON (600 mg/1)
Marketing started20191216
Package count1

External sources

Source: openFDA. Public-domain (CC0).