NDC 72789-565
Ibuprofen 800 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 11788-010.
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
- 800 mg
- Approval
- ANDA ANDA202413
- On the market since
- Dec 15, 2025
- Package NDCs
72789-565-1072789-565-1572789-565-2172789-565-3072789-565-4072789-565-6072789-565-8272789-565-8672789-565-9072789-565-9372789-565-94- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2026
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