Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 60 mg
- Approval
- ANDA ANDA090739
- On the market since
- May 27, 2014
- Package NDCs
65841-801-0665841-801-1065841-801-16- Official label
- DailyMed (National Library of Medicine), updated Nov 28, 2024
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