FDA NDC Directory · JSON-LD · Markdown

FEBUXOSTAT

NDC 0527-2244 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefebuxostat
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213069
Dosage form / routeTABLET · ORAL
Active ingredientsFEBUXOSTAT (40 mg/1)
Marketing started20200602
Package count1

External sources

Source: openFDA. Public-domain (CC0).