NDC 68788-4006
Fenofibrate 145 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-389.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
| Lupin Limited | Pithampur, India | Makes it and packages it | Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action |
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 145 mg
- Approval
- ANDA ANDA090856
- On the market since
- Aug 8, 2025
- Package NDCs
68788-4006-168788-4006-368788-4006-668788-4006-9- Official label
- DailyMed (National Library of Medicine), updated Aug 8, 2025
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