NDC 68071-2369
Fenofibrate 48 mg tablet, coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-768.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, coated, oral
- Strength
- 48 mg
- Approval
- ANDA ANDA205118
- On the market since
- May 5, 2016
- Package NDCs
68071-2369-9- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2026
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