NDC 71205-530

Nabumetone 750 mg tablet

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-466.

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
750 mg
Approval
ANDA ANDA078420
On the market since
Jun 26, 2019
Package NDCs
71205-530-30 71205-530-60 71205-530-90
Official label
DailyMed (National Library of Medicine), updated Apr 1, 2022

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