NDC 72189-607

Lubiprostone 24 ug capsule, gelatin coated

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-352.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Catalent Pharma Solutions, LLCSt Petersburg, FL, United StatesMakes it and tests it Problems found, fixed voluntarilyJan 30, 2026 · 9 inspections

Repackaging site

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
Jan 16, 2025
Package NDCs
72189-607-60
Official label
DailyMed (National Library of Medicine), updated Jan 16, 2025

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