FDA NDC Directory · JSON-LD · Markdown

Voriconazole

NDC 60687-968 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA206837
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (50 mg/1)
Marketing started20260827
Package count1

External sources

Source: openFDA. Public-domain (CC0).