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Fidaxomicin

NDC 0054-0795 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerHikma Pharmceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219737
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFIDAXOMICIN (200 mg/1)
Marketing started20261007
Package count1

External sources

Source: openFDA. Public-domain (CC0).