NDC 59651-217
Fenofibric Acid 135 mg capsule, delayed release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 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 ANDA212598
- On the market since
- Jul 25, 2019
- Package NDCs
59651-217-90- Official label
- DailyMed (National Library of Medicine), updated Aug 2, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?