NDC 42291-931
Ursodiol 500 mg tablet, film coated
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from ENDO USA, Inc.'s NDC 49884-413.
Where the pills inside were 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
- Dec 14, 2023
- Package NDCs
42291-931-01- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
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