NDC 72789-310
Fenofibrate 130 mg capsule
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-444.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ohm Laboratories Inc. | New Brunswick, NJ, United States | Makes it | No problems foundOct 31, 2024 · 22 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, oral
- Strength
- 130 mg
- Approval
- ANDA ANDA201748
- On the market since
- Mar 2, 2015
- Package NDCs
72789-310-30- Official label
- DailyMed (National Library of Medicine), updated Feb 26, 2026
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