NDC 67046-1451
Duloxetine 30 mg capsule, delayed release
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-595.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Chhatrapati Sambhajinagar, India | Makes it | Problems found, fixed voluntarilyApr 21, 2026 · 6 inspections |
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA208706
- On the market since
- Feb 7, 2025
- Package NDCs
67046-1451-3- Official label
- DailyMed (National Library of Medicine), updated Feb 7, 2025
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