NDC 60687-606
Diclofenac Sodium 50 mg tablet, delayed release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-202.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it | Problems found, fixed voluntarilyOct 23, 2022 · 6 inspections |
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it | No problems foundMar 7, 2025 · 2 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA090066
- On the market since
- Jun 7, 2022
- Package NDCs
60687-606-0160687-606-11- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
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