NDC 68071-3451
Diclofenac Potassium 50 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1832.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA215750
- On the market since
- May 12, 2022
- Package NDCs
68071-3451-3- Official label
- DailyMed (National Library of Medicine), updated Feb 5, 2025
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