NDC 71335-2654
Fenofibrate 48 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-595.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Hyderabad, India | Makes it | Problems found, fixed voluntarilyJul 21, 2023 · 8 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Sep 12, 2018 · Class III · Hetero Labs, Ltd. - Unit III
Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.
Lots: Lot #: E181370, Exp. 5/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 48 mg
- Approval
- ANDA ANDA204598
- On the market since
- Jul 14, 2016
- Package NDCs
71335-2654-171335-2654-271335-2654-3- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2025
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