NDC 69339-163
Lubiprostone 24 ug capsule, gelatin coated
On the label: Natco Pharma USA LLC. It's repackaged: Natco Pharma USA LLC rebottles it from ENDO USA, Inc.'s NDC 0254-3029.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.
Repackaging site
- Apace Packaging LLC, Fountain Run, KY, 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
- Oct 17, 2022
- Package NDCs
69339-163-1769339-163-98- Official label
- DailyMed (National Library of Medicine), updated Dec 22, 2025
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