NDC 76420-906
Lubiprostone 8 ug capsule, gelatin coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-351.
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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
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
76420-906-0176420-906-3076420-906-6076420-906-90- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2025
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