FDA NDC Directory · JSON-LD · Markdown

PRUCALOPRIDE

NDC 62332-078 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219234
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPRUCALOPRIDE SUCCINATE (2 mg/1)
Marketing started20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).