NDC 85534-0013
Ibuprofen 800 mg tablet
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, 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
- May 8, 2020
- Package NDCs
85534-0013-085534-0013-185534-0013-285534-0013-3- Official label
- DailyMed (National Library of Medicine), updated Jun 26, 2026
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