NDC 82868-101
Diclofenac Sodium 50 mg tablet, delayed release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals 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
- Northwind Health Company, LLC, Indianapolis, IN, 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
- Feb 12, 2026
- Package NDCs
82868-101-3082868-101-90- Official label
- DailyMed (National Library of Medicine), updated Aug 19, 2026
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