FDA NDC Directory · JSON-LD · Markdown

Voriconazole

NDC 50268-803 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAvPAK
Marketing categoryAbbreviated NDA (generic) · App ANDA206654
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsVORICONAZOLE (200 mg/1)
Marketing started20220819
Package count1

External sources

Source: openFDA. Public-domain (CC0).