NDC 68071-2333

Naproxen Sodium 550 mg tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-433.

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
Naproxen: every company that makes it
Form
tablet, oral
Strength
550 mg
Approval
ANDA ANDA212199
On the market since
Oct 30, 2019
Package NDCs
68071-2333-2 68071-2333-3 68071-2333-4
Official label
DailyMed (National Library of Medicine), updated Jan 3, 2025

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