NDC 0406-6301

Prucalopride 1 mg tablet, film coated

On the label: SpecGx LLC.

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants SpecGx LLC names for other drugs.

Product details

Generic drug
Prucalopride: every company that makes it
Form
tablet, film coated, oral
Strength
1 mg
Approval
ANDA ANDA219193
On the market since
Jun 24, 2025
Package NDCs
0406-6301-03
Official label
DailyMed (National Library of Medicine), updated Jan 23, 2026

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