NDC 49884-413

Ursodiol 500 mg tablet, film coated

On the label: ENDO USA, Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.

Product details

Generic drug
Ursodiol: every company that makes it
Form
tablet, film coated, oral
Strength
500 mg
Approval
ANDA ANDA202540
On the market since
Aug 1, 2013
Package NDCs
49884-413-01 49884-413-05
Official label
DailyMed (National Library of Medicine), updated Jun 12, 2026

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