NDC 54868-5994
Fenofibrate 134 mg capsule
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Amneal Pharmaceuticals's NDC 0115-0522.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
Recalls
- Mar 17, 2016 · Class III · Impax Laboratories, Inc.
Labeling: Incorrect or Missing Lot and/or Exp. Date
Lots: Lot # 10008624, 10008831; Exp. 10/16 Lot # 10009339; Exp. 02/17 Lot # 10009566,10009627; Exp. 04/17 Lot # 10010200, 20001419A, 20001426A; Exp. 10/17 Lot # 20001732A; Exp. 04/18 Lot # 20001790A, 20001791A, 20001792A; Exp. 05/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fenofibrate: every company that makes it
- Form
- capsule
- Strength
- 134 mg
- Approval
- ANDA ANDA075868
- On the market since
- Feb 25, 2009
- Package NDCs
54868-5994-054868-5994-1- Official label
- DailyMed (National Library of Medicine), updated May 25, 2010
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