NDC 68071-5319
Diclofenac Sodium 50 mg tablet, delayed release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-842.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA075281
- On the market since
- Apr 17, 2025
- Package NDCs
68071-5319-1- Official label
- DailyMed (National Library of Medicine), updated Sep 2, 2026
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