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Voriconazole

NDC 31722-266 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211598
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsVORICONAZOLE (40 mg/mL)
Marketing started20250808
Package count1

External sources

Source: openFDA. Public-domain (CC0).