NDC 51655-866
Fenofibrate 48 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Cipla USA., Inc.'s NDC 69097-459.
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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 48 mg
- Approval
- ANDA ANDA208709
- On the market since
- Jul 10, 2023
- Package NDCs
51655-866-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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