FDA NDC Directory · JSON-LD · Markdown

Ursodiol

NDC 72162-1501 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA202540
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsURSODIOL (500 mg/1)
Marketing started20130801
Package count1

External sources

Source: openFDA. Public-domain (CC0).