Quick answers
- What is Seladelpar lysine used for?
- The FDA-approved label (Livdelzi, Gilead Sciences, Inc, February 3, 2026) says: “LIVDELZI is indicated for the treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults who have had an inadequate response to UDCA, or as monotherapy in patients unable to tolerate UDCA. This indication is approved under accelerated approval based on a reduction of alkaline phosphatase (ALP) […]. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Seladelpar lysine have a boxed warning?
- No. None of the 1 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Seladelpar lysine?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Seladelpar lysine been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Seladelpar lysine?
- 1 company lists prescription products of Seladelpar lysine in the FDA NDC Directory, including Gilead Sciences, Inc..
What Seladelpar lysine is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
LIVDELZI is indicated for the treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults who have had an inadequate response to UDCA, or as monotherapy in patients unable to tolerate UDCA. This indication is approved under accelerated approval based on a reduction of alkaline phosphatase (ALP) […]. …
— FDA label: Livdelzi, Gilead Sciences, Inc, effective February 3, 2026. Read the full label on DailyMed →
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
Forms and how it is given
| Dosage forms | Capsule |
|---|---|
| Route | Oral |
| Prescription products | 1 in the FDA NDC Directory |
| Brand names | Livdelzi |
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Gilead Sciences, Inc.1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA217899 LIVDELZI | Gilead Sciences Inc | August 14, 2024 | 1, latest January 30, 2026 2026: Labeling |
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 2690875, 2690881 |
|---|---|
| SPL set ID of the quoted label | 89f79d98-135c-40b2-a585-6996c04e599c |
| FDA labels (SPL) | 1 |
| FDA applications | NDA217899 |
| Active ingredients (FDA) | SELADELPAR LYSINE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Livdelzi, Gilead Sciences, Inc, effective February 3, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- 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 recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →