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Ursodiol

NDC 68462-474 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA090801
Dosage form / routeTABLET · ORAL
Active ingredientsURSODIOL (500 mg/1)
Marketing started20110712
Package count3

External sources

Source: openFDA. Public-domain (CC0).