NDC 68071-1712
fenofibrate 145 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Leading Pharma, LLC's NDC 69315-288.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Graviti Pharmaceuticals Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 145 mg
- Approval
- ANDA ANDA211122
- On the market since
- Jul 18, 2022
- Package NDCs
68071-1712-9- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2025
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