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Voriconazole

NDC 65862-892 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206837
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (200 mg/1)
Marketing started20160122
Package count4

External sources

Source: openFDA. Public-domain (CC0).