NDC 50090-4373
Fenofibric acid 135 mg capsule, delayed release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-129.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, delayed release
- Strength
- 135 mg
- Approval
- ANDA ANDA200750
- On the market since
- Dec 4, 2013
- Package NDCs
50090-4373-0- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2021
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