NDC 63304-351
Lubiprostone 8 ug capsule, gelatin coated
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's 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 |
Product details
- Generic drug
- Lubiprostone: every company that makes it
- Form
- capsule, gelatin coated, oral
- Strength
- 8 ug
- Approval
- NDA authorized generic NDA021908
- On the market since
- Jan 1, 2023
- Package NDCs
63304-351-60- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?