NDC 63304-352

Lubiprostone 24 ug capsule, gelatin coated

On the label: Caraco Pharmaceutical Laboratories, Ltd..

United States: 1

Where it's made

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

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 1, 2023
Package NDCs
63304-352-60
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?