NDC 69367-330

Pregabalin 225 mg capsule

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Pregabalin: every company that makes it
Form
capsule, oral
Strength
225 mg
Approval
ANDA ANDA208677
On the market since
Aug 24, 2021
Package NDCs
69367-330-09
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2025

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