NDC 87063-223
Diclofenac Sodium 20 mg per 1 g solution
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-537.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Pithampur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 17, 2025 · 3 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, 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 ANDA208021
- On the market since
- Feb 19, 2024
- Package NDCs
87063-223-04- Official label
- DailyMed (National Library of Medicine), updated Jun 10, 2026
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