NDC 76420-009

celecoxib 200 mg capsule

On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-157.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedDistrict Solan, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action

Repackaging site

Product details

Generic drug
Celecoxib: every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA204590
On the market since
Mar 16, 2016
Package NDCs
76420-009-01 76420-009-07 76420-009-14 76420-009-20 76420-009-30 76420-009-60 76420-009-90
Official label
DailyMed (National Library of Medicine), updated Sep 2, 2023

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