NDC 75834-338
Diclofenac Potassium 50 mg powder, for solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it and tests 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
- Dec 15, 2025
- Package NDCs
75834-338-0175834-338-02- Official label
- DailyMed (National Library of Medicine), updated Oct 26, 2026
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