NDC 71335-1701
Fenofibrate 48 mg tablet, coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 65862-768.
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 |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, coated, oral
- Strength
- 48 mg
- Approval
- ANDA ANDA205118
- On the market since
- May 5, 2016
- Package NDCs
71335-1701-171335-1701-271335-1701-3- Official label
- DailyMed (National Library of Medicine), updated Sep 25, 2025
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