NDC 80425-0355
Lubiprostone 24 ug capsule, gelatin coated
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-352.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Catalent Pharma Solutions, LLC | St Petersburg, FL, United States | Makes it and tests it | Problems found, fixed voluntarilyJan 30, 2026 · 9 inspections |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Lubiprostone: every company that makes it
- Form
- capsule, gelatin coated, oral
- Strength
- 24 ug
- Approval
- NDA authorized generic NDA021908
- On the market since
- Aug 16, 2023
- Package NDCs
80425-0355-2- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2024
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