NDC 67296-2345

Ibuprofen 800 mg tablet, film coated

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from AiPing Pharmaceutical, Inc.'s NDC 11788-010.

China: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Anshi Pharmaceutical (Zhongshan) Inc.Zhongshan, ChinaMakes it Problems found, fixed voluntarilyOct 27, 2017 · 3 inspections
Shandong Xinhua Pharmaceutical Co., Ltd. FDF PlantZibo, ChinaMakes it No problems foundDec 8, 2023 · 2 inspections

Repackaging site

Product details

Generic drug
Ibuprofen: every company that makes it
Form
tablet, film coated, oral
Strength
800 mg
Approval
ANDA ANDA202413
On the market since
Dec 15, 2025
Package NDCs
67296-2345-3
Official label
DailyMed (National Library of Medicine), updated Oct 20, 2026

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