Quick answers
- What is Urso 250?
- Urso 250 is a brand name of Ursodiol, a prescription medicine. The FDA NDC Directory lists 1 Urso 250 product in 1 strength and form.
- Who makes Urso 250?
- Abbvie holds the FDA application for Urso 250 (NDA020675, approved December 10, 1997).
- Is there a generic or store brand of Urso 250?
- Yes. The FDA NDC Directory lists 5 other products with the same active ingredients, strength and form as a Urso 250 product, 5 of them generic. Ask your pharmacist whether one is right for you.
- Has Urso 250 been recalled?
- No recall linked to Urso 250 products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Urso 250 is
Each Urso 250 product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Ursodiol · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| ursodiol 250 mg tablet, film coated (oral) | Urso 250 | 5 products, 4 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Ursodiol →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020675 | Abbvie | December 10, 1997 | 1 |
Companies that list Urso 250
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Urso 250 products.
- Allergan, Inc.1 product
Recalls
No recall linked to Urso 250 products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.