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Prucalopride

NDC 70954-596 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218492
Dosage form / routeTABLET · ORAL
Active ingredientsPRUCALOPRIDE SUCCINATE (1 mg/1)
Marketing started20241226
Package count1

External sources

Source: openFDA. Public-domain (CC0).