NDC 71335-3086
Fenofibrate 160 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 59651-576.
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, film coated, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA216798
- On the market since
- Sep 27, 2022
- Package NDCs
71335-3086-171335-3086-271335-3086-371335-3086-471335-3086-5- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?