NDC 33342-161
Duloxetine Hydrochloride 30 mg capsule, delayed release
On the label: Macleods Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA204815
- On the market since
- Mar 24, 2017
- Package NDCs
33342-161-0733342-161-1033342-161-1233342-161-44- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2025
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