NDC 70518-4721
Fenofibrate 54 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-575.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 54 mg
- Approval
- ANDA ANDA216798
- On the market since
- Aug 4, 2026
- Package NDCs
70518-4721-0- Official label
- DailyMed (National Library of Medicine), updated Aug 4, 2026
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