NDC 68071-5101
Fenofibrate 145 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Cipla USA., Inc.'s NDC 69097-458.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Indore, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 17, 2023 · 6 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, oral
- Strength
- 145 mg
- Approval
- ANDA ANDA208709
- On the market since
- Dec 15, 2016
- Package NDCs
68071-5101-9- Official label
- DailyMed (National Library of Medicine), updated Jun 19, 2024
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