FDA NDC Directory · JSON-LD · Markdown

voriconazole

NDC 72578-063 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerViona Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA206747
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (200 mg/1)
Marketing started20190416
Package count6

External sources

Source: openFDA. Public-domain (CC0).