NDC 53002-5370
Diclofenac Sodium Delayed Release 50 mg tablet, delayed release
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-102.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release
- Strength
- 50 mg
- Approval
- ANDA ANDA075185
- On the market since
- Nov 13, 1998
- Package NDCs
53002-5370-3- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
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