NDC 60687-816
Lubiprostone 8 ug capsule, gelatin coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Teva Pharmaceuticals, Inc.'s NDC 0480-3479.
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 Teva Pharmaceuticals, Inc. names for other drugs.
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Lubiprostone: every company that makes it
- Form
- capsule, gelatin coated, oral
- Strength
- 8 ug
- Approval
- ANDA ANDA209920
- On the market since
- Mar 18, 2026
- Package NDCs
60687-816-3260687-816-33- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2026
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