NDC 68071-4231
Diclofenac SodiumDelayed Release 50 mg tablet, delayed release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- 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 ANDA075185
- On the market since
- Nov 13, 1998
- Package NDCs
68071-4231-168071-4231-368071-4231-568071-4231-668071-4231-9- Official label
- DailyMed (National Library of Medicine), updated Jun 6, 2024
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