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Voriconazole

NDC 0378-1626 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namevoriconazole
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090547
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (50 mg/1)
Marketing started20110215
Package count1

External sources

Source: openFDA. Public-domain (CC0).