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Voriconazole

NDC 27241-063 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206181
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (200 mg/1)
Marketing started20160531
Package count1

External sources

Source: openFDA. Public-domain (CC0).