NDC 68180-129
Fenofibric acid 135 mg capsule, delayed release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 135 mg
- Approval
- ANDA ANDA200750
- On the market since
- Dec 4, 2013
- Package NDCs
68180-129-0168180-129-0268180-129-09- Official label
- DailyMed (National Library of Medicine), updated Dec 8, 2023
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