NDC 68071-2387

Gemfibrozil 600 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-128.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Repackaging site

Product details

Generic drug
Gemfibrozil: every company that makes it
Form
tablet, oral
Strength
600 mg
Approval
ANDA ANDA214603
On the market since
Jan 20, 2021
Package NDCs
68071-2387-3 68071-2387-6 68071-2387-8
Official label
DailyMed (National Library of Medicine), updated Mar 5, 2026

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