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Prucalopride

NDC 0406-6302 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSpecGx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219193
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRUCALOPRIDE (2 mg/1)
Marketing started20250624
Package count1

External sources

Source: openFDA. Public-domain (CC0).