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Voriconazole

NDC 70594-067 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerXellia Pharmaceuticals USA LLC
Marketing categoryNew Drug Application (innovator) · App NDA208562
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVORICONAZOLE (10 mg/mL)
Marketing started20230824
Package count1

External sources

Source: openFDA. Public-domain (CC0).