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Prucalopride

NDC 69238-2698 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218812
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRUCALOPRIDE SUCCINATE (1 mg/1)
Marketing started20240930
Package count1

External sources

Source: openFDA. Public-domain (CC0).