NDC 42291-230
Diclofenac Sodium 50 mg tablet, delayed release
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-102.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA075185
- On the market since
- Mar 17, 2011
- Package NDCs
42291-230-1042291-230-18- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
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