Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Chhatrapati Sambhajinagar, India | Makes it | Problems found, fixed voluntarilyApr 21, 2026 · 6 inspections |
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Recalls
- May 28, 2026 · Class II · Ajanta Pharma USA Inc
CGMP Deviations
Lots: Lot # PA02216; Exp. 12/2029 - Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: PA03410
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
- capsule, oral
- Strength
- 67 mg
- Approval
- ANDA ANDA210705
- On the market since
- Sep 10, 2018
- Package NDCs
27241-118-0427241-118-05- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2025
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