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Voriconazole

NDC 65219-190 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211099
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVORICONAZOLE (10 mg/mL)
Marketing started20201201
Package count1

External sources

Source: openFDA. Public-domain (CC0).