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Voriconazole

NDC 43547-377 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerSolco Healthcare U.S., LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206654
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsVORICONAZOLE (50 mg/1)
Marketing started20161028
Package count2

External sources

Source: openFDA. Public-domain (CC0).