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Mifepristone

NDC 84670-014 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMIFEPRISTONE
Labeler / ManufacturerEvita Solutions LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216616
Dosage form / routeTABLET · ORAL
Active ingredientsMIFEPRISTONE (200 mg/1)
Marketing started20250930
Package count1

External sources

Source: openFDA. Public-domain (CC0).