NDC 0615-8270
fenofibrate 160 mg tablet
On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-117.
Where the pills inside were 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 |
Repackaging site
- NCS HealthCare of KY, LLC dba Vangard Labs, Glasgow, KY, United States · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA210138
- On the market since
- Jul 20, 2018
- Package NDCs
0615-8270-39- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2019
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