FDA NDC Directory · JSON-LD · Markdown

OXBRYTA

NDC 72786-101 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameVoxelotor
Labeler / ManufacturerGlobal Blood Therapeutics, Inc, A subsidiary of Pfizer Inc.
Marketing categoryNew Drug Application (innovator) · App NDA213137
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVOXELOTOR (500 mg/1)
Marketing started20191125
Package count1

External sources

Source: openFDA. Public-domain (CC0).