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Ursodiol

NDC 55154-2633 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCardinal Health 107, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202540
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsURSODIOL (250 mg/1)
Marketing started20241031
Package count1

External sources

Source: openFDA. Public-domain (CC0).