NDC 70934-223
Fenofibrate 160 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Amneal Pharmaceuticals's NDC 0115-5522.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals of New York, LLC | Brookhaven, NY, United States | Makes it, tests it, packages it and labels it | No problems foundSep 25, 2026 · 14 inspections |
| Reed-Lane, Inc. | Wayne, NJ, United States | Packages it | No problems foundOct 17, 2025 · 7 inspections |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet
- Strength
- 160 mg
- Approval
- ANDA ANDA076509
- On the market since
- Jan 9, 2019
- Package NDCs
70934-223-3070934-223-60- Official label
- DailyMed (National Library of Medicine), updated May 6, 2021
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