NDC 60687-864
Fenofibrate 160 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Rhodes Pharmaceuticals L.P.'s NDC 42858-660.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Adare Pharmaceuticals, Inc. | Vandalia, OH, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2025 · 8 inspections |
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it, tests it and packages it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA076433
- On the market since
- Apr 19, 2025
- Package NDCs
60687-864-1160687-864-21- Official label
- DailyMed (National Library of Medicine), updated Apr 19, 2025
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