NDC 0781-8159

Prucalopride 2 mg tablet, film coated

On the label: Sandoz Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Appco Pharma LLCPiscataway, NJ, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections

Product details

Generic drug
Prucalopride: every company that makes it
Form
tablet, film coated, oral
Strength
2 mg
Approval
ANDA ANDA218963
On the market since
Jun 13, 2025
Package NDCs
0781-8159-31
Official label
DailyMed (National Library of Medicine), updated Sep 2, 2025

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