NDC 70518-2907
Fenofibrate 160 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Lifestar Pharma LLC.'s NDC 70756-215.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 2 inspections |
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA213864
- On the market since
- Oct 13, 2020
- Package NDCs
70518-2907-070518-2907-1- Official label
- DailyMed (National Library of Medicine), updated Jul 30, 2026
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