NDC 53002-3068

Gemfibrozil 600 mg tablet, film coated

On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-784.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Gemfibrozil: every company that makes it
Form
tablet, film coated
Strength
600 mg
Approval
ANDA ANDA202726
On the market since
Sep 16, 2015
Package NDCs
53002-3068-0 53002-3068-6
Official label
DailyMed (National Library of Medicine), updated Aug 10, 2023

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