NDC 76420-210

Nabumetone 500 mg tablet

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-465.

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
Nabumetone: every company that makes it
Form
tablet, oral
Strength
500 mg
Approval
ANDA ANDA078420
On the market since
Jun 26, 2019
Package NDCs
76420-210-07 76420-210-10 76420-210-14 76420-210-20 76420-210-30 76420-210-60
Official label
DailyMed (National Library of Medicine), updated Mar 7, 2022

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