NDC 82009-170
Duloxetine 20 mg capsule, delayed release
On the label: Quallent Pharmaceuticals Health LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Bharuch, India | Makes it | No problems foundJun 23, 2023 · 3 inspections |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA208706
- On the market since
- Jul 1, 2025
- Package NDCs
82009-170-10- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2025
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