NDC 68001-377

Ursodiol 250 mg tablet

On the label: BluePoint Laboratories..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action

Product details

Generic drug
Ursodiol: every company that makes it
Form
tablet, oral
Strength
250 mg
Approval
ANDA ANDA090801
On the market since
Feb 26, 2019
Package NDCs
68001-377-00
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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