NDC 0615-8495
Duloxetine 30 mg capsule, delayed release
On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-295.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- NCS HealthCare of KY, LLC dba Vangard Labs, Glasgow, KY, United States · repackages it
Recalls
- Nov 21, 2017 · Class III · Lupin Pharmaceuticals Inc.
Failed Dissolution Specification
Lots: Lot #: G602051, Exp. 12/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Duloxetine: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA090694
- On the market since
- Dec 11, 2013
- Package NDCs
0615-8495-050615-8495-39- Official label
- DailyMed (National Library of Medicine), updated Jan 3, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?