NDC 76420-778
Lubiprostone 24 ug capsule
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1642.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
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, oral
- Strength
- 24 ug
- Approval
- ANDA ANDA214131
- On the market since
- Mar 23, 2023
- Package NDCs
76420-778-0176420-778-3076420-778-6076420-778-90- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2025
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