NDC 68788-7816
Fenofibrate 160 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Lifestar Pharma LLC.'s NDC 70756-215.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 2 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
- 160 mg
- Approval
- ANDA ANDA213864
- On the market since
- Nov 6, 2020
- Package NDCs
68788-7816-368788-7816-9- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
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