NDC 68001-368
Duloxetine Delayed-Release 40 mg capsule, delayed release pellets
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Towa Pharmaceutical Europe, S.L. | Martorelles, Spain | Makes it | Problems found, fixed voluntarilySep 9, 2022 · 6 inspections |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release pellets, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA203088
- On the market since
- May 21, 2018
- Package NDCs
68001-368-04- Official label
- DailyMed (National Library of Medicine), updated Feb 14, 2024
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