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Chenodal

NDC 68974-876 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameChenodiol
Labeler / ManufacturerTravere Therapeutics
Marketing categoryAbbreviated NDA (generic) · App ANDA091019
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCHENODIOL (250 mg/1)
Marketing started20151228
Marketing ended20261130
Package count1

External sources

Source: openFDA. Public-domain (CC0).