NDC 71610-754

Pregabalin 200 mg capsule

On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-355.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Pregabalin: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA208677
On the market since
Jul 19, 2019
Package NDCs
71610-754-30 71610-754-46 71610-754-53
Official label
DailyMed (National Library of Medicine), updated Nov 28, 2023

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