NDC 80425-0012
Duloxetine HCLDR 30 mg capsule, delayed release
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Ascend Laboratories, LLC's NDC 67877-264.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Amaliya Daman, India | Makes it, tests it and packages it | No problems foundAug 30, 2019 · 6 inspections |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA203197
- On the market since
- May 1, 2012
- Package NDCs
80425-0012-180425-0012-2- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
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