NDC 76420-842

Celecoxib 50 mg capsule

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-156.

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
Celecoxib: every company that makes it
Form
capsule, oral
Strength
50 mg
Approval
ANDA ANDA205129
On the market since
Dec 3, 2020
Package NDCs
76420-842-00 76420-842-01 76420-842-07 76420-842-14 76420-842-20 76420-842-30 76420-842-60 76420-842-90
Official label
DailyMed (National Library of Medicine), updated Apr 11, 2025

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