NDC 85509-1369
Diclofenac Sodium 20 mg per 1 g solution
On the label: Phoenix RX LLC. It's repackaged: Phoenix RX LLC rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-1369.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Repackaging site
- Phoenix RX LLC, Hatboro, PA, United States · relabels it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- solution, topical
- Strength
- 20 mg per 1 g
- Approval
- ANDA ANDA208098
- On the market since
- May 31, 2023
- Package NDCs
85509-1369-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2025
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