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PRUCALOPRIDE

NDC 0781-8159 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSandoz Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218963
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRUCALOPRIDE SUCCINATE (2 mg/1)
Marketing started20250613
Package count1

External sources

Source: openFDA. Public-domain (CC0).