NDC 68071-3542
Fenofibrate 160 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-576.
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, film coated, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA216798
- On the market since
- Sep 27, 2022
- Package NDCs
68071-3542-9- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2025
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