NDC 47335-381
Duloxetine 20 mg capsule, delayed release
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's 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 |
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090745
- On the market since
- Dec 11, 2013
- Package NDCs
47335-381-0847335-381-1847335-381-6147335-381-8347335-381-8647335-381-88- Official label
- DailyMed (National Library of Medicine), updated Nov 8, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?