NDC 76420-670
Diclofenac Sodium 75 mg tablet, delayed release
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-201.
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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Diclofenac: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA077863
- On the market since
- Aug 19, 2008
- Package NDCs
76420-670-0076420-670-0176420-670-0576420-670-3076420-670-6076420-670-90- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2026
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