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Mifepristone

NDC 76346-654 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCorcept Therapeutics Incorporated
Marketing categoryNew Drug Application (innovator) · App NDA202107
Dosage form / routeTABLET · ORAL
Active ingredientsMIFEPRISTONE (300 mg/1)
Marketing started20240528
Package count1

External sources

Source: openFDA. Public-domain (CC0).