NDC 60290-061
Diclofenac Potassium 50 mg powder, for solution
On the label: Umedica Laboratories USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections |
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- powder, for solution, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA217010
- On the market since
- Feb 15, 2026
- Package NDCs
60290-061-0160290-061-02- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?