FDA NDC Directory · JSON-LD · Markdown

VEOZAH

NDC 0469-2760 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefezolinetant
Labeler / ManufacturerAstellas Pharma US, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA216578
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEZOLINETANT (45 mg/1)
Marketing started20230512
Package count1

External sources

Source: openFDA. Public-domain (CC0).