NDC 61919-636
Duloxetine 20 mg capsule, delayed release
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-381.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA090745
- On the market since
- Feb 20, 2017
- Package NDCs
61919-636-2061919-636-60- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2017
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