NDC 70518-2902
Ibuprofen 600 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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
- Oct 6, 2020
- Package NDCs
70518-2902-070518-2902-170518-2902-2- Official label
- DailyMed (National Library of Medicine), updated Aug 26, 2026
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