FDA NDC Directory · JSON-LD · Markdown

ZEGFROVY

NDC 84694-102 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameSunvozertinib
Labeler / ManufacturerDizal Pharmaceutical Co., Ltd.
Marketing categoryNew Drug Application (innovator) · App NDA219839
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSUNVOZERTINIB (200 mg/1)
Marketing started20261022
Package count1

External sources

Source: openFDA. Public-domain (CC0).