FDA NDC Directory · JSON-LD · Markdown

Ursodiol

NDC 60687-527 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA211145
Dosage form / routeTABLET · ORAL
Active ingredientsURSODIOL (250 mg/1)
Marketing started20200911
Package count1

External sources

Source: openFDA. Public-domain (CC0).