NDC 71205-831

Lubiprostone 8 ug capsule, gelatin coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 63304-351.

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
8 ug
Approval
NDA authorized generic NDA021908
On the market since
Jan 1, 2023
Package NDCs
71205-831-00 71205-831-11 71205-831-30 71205-831-55 71205-831-60 71205-831-64 71205-831-67 71205-831-72 71205-831-78 71205-831-90
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2023

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