NDC 70247-012
duloxetine 20 mg capsule, delayed release
On the label: Qingdao BAHEAL Pharmaceutical Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qingdao BAHEAL Pharmaceutical Co.,Ltd. | Qingdao, China | Makes it | No problems foundMar 22, 2024 · 2 inspections |
| Sci Pharmtech, Inc. | Taoyuan City, Taiwan | Makes the active ingredient | Problems found, fixed voluntarilyJun 6, 2025 · 5 inspections |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA210599
- On the market since
- May 5, 2018
- Package NDCs
70247-012-06- Official label
- DailyMed (National Library of Medicine), updated Nov 11, 2025
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