NDC 72789-598
Ibuprofen 600 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from AiPing Pharmaceutical, Inc.'s NDC 11788-009.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Anshi Pharmaceutical (Zhongshan) Inc. | Zhongshan, China | Makes it | Problems found, fixed voluntarilyOct 27, 2017 · 3 inspections |
| Shandong Xinhua Pharmaceutical Co., Ltd. FDF Plant | Zibo, China | Makes it | No problems foundDec 8, 2023 · 2 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA202413
- On the market since
- Dec 15, 2025
- Package NDCs
72789-598-0172789-598-1572789-598-8272789-598-90- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2026
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