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voriconazole

NDC 70436-230 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerSlate Run Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216805
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsVORICONAZOLE (40 mg/mL)
Marketing started20240301
Package count1

External sources

Source: openFDA. Public-domain (CC0).