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Ursodiol

NDC 70710-1127 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211145
Dosage form / routeTABLET · ORAL
Active ingredientsURSODIOL (250 mg/1)
Marketing started20181107
Package count2

External sources

Source: openFDA. Public-domain (CC0).