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Fluconazole

NDC 70518-4020 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA077731
Dosage form / routeTABLET · ORAL
Active ingredientsFLUCONAZOLE (200 mg/1)
Marketing started20240212
Package count2

External sources

Source: openFDA. Public-domain (CC0).