NDC 68071-2939

Ibuprofen 400 mg tablet, film coated

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Florida Pharmaceutical Products, LLC.'s NDC 71921-180.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Contract Pharmacal Corp.Hauppauge, NY, United StatesMakes it Problems found, fixed voluntarilyApr 14, 2022 · 13 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Ibuprofen: every company that makes it
Form
tablet, film coated, oral
Strength
400 mg
Approval
ANDA ANDA071268
On the market since
Oct 21, 2021
Package NDCs
68071-2939-4 68071-2939-6
Official label
DailyMed (National Library of Medicine), updated Dec 13, 2024

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