NDC 55289-150
Diclofenac Sodium 75 mg tablet, delayed release
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Actavis Pharma, Inc.'s NDC 0228-2551.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Actavis Elizabeth LLC | Elizabeth, New Jersey, United States | Makes it | No problems foundJul 24, 2023 · 16 inspections |
| Actavis Laboratories UT, Inc. | Salt Lake City, UT, United States | Labels it | Problems found, fixed voluntarilySep 19, 2025 · 12 inspections, 1 with FDA action |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA074514
- On the market since
- Mar 26, 1996
- Package NDCs
55289-150-1055289-150-1555289-150-2055289-150-2855289-150-3055289-150-60- Official label
- DailyMed (National Library of Medicine), updated May 5, 2025
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