FDA NDC Directory · JSON-LD · Markdown

voriconazole

NDC 63629-8734 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA200265
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (200 mg/1)
Marketing started20111212
Package count1

External sources

Source: openFDA. Public-domain (CC0).