NDC 62332-278
Duloxetine Hydrochloride 20 mg capsule, delayed release
On the label: Alembic Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA202949
- On the market since
- Apr 9, 2026
- Package NDCs
62332-278-3062332-278-6062332-278-9062332-278-91- Official label
- DailyMed (National Library of Medicine), updated May 6, 2026
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