NDC 70518-4010
Ibuprofen 800 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-362.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Product details
- Generic drug
- Ibuprofen: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA213794
- On the market since
- Feb 5, 2024
- Package NDCs
70518-4010-070518-4010-170518-4010-2- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?