NDC 60687-713
Fenofibrate 200 mg capsule
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-582.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Mar 13, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Lots: Lot # 17230834, exp. date Mar-25 17230835, exp. date Mar-25
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA205566
- On the market since
- Mar 13, 2023
- Package NDCs
60687-713-1160687-713-21- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2026
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