NDC 70710-1641

Lubiprostone 8 ug capsule

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Lubiprostone: every company that makes it
Form
capsule, oral
Strength
8 ug
Approval
ANDA ANDA214131
On the market since
Mar 23, 2023
Package NDCs
70710-1641-1 70710-1641-6
Official label
DailyMed (National Library of Medicine), updated Mar 27, 2023

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