NDC 72603-288

Lubiprostone 0.008 mg capsule

On the label: Northstar Rx LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Lubiprostone: every company that makes it
Form
capsule, oral
Strength
0.008 mg
Approval
ANDA ANDA218640
On the market since
Jul 1, 2025
Package NDCs
72603-288-01
Official label
DailyMed (National Library of Medicine), updated Jun 25, 2025

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