Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Prescription medicine

Fostamatinib

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Fostamatinib used for?
The FDA-approved label (Tavalisse, Rigel Pharmaceuticals, Inc., November 5, 2025) says: “TAVALISSE is indicated for the treatment of thrombocytopenia in adult patients with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment. TAVALISSE is a kinase inhibitor indicated for the treatment of thrombocytopenia in adult patients with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Fostamatinib 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 Fostamatinib?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Fostamatinib been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Fostamatinib?
1 company lists prescription products of Fostamatinib in the FDA NDC Directory, including Rigel Pharmaceuticals, Inc..

What Fostamatinib is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

TAVALISSE is indicated for the treatment of thrombocytopenia in adult patients with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment. TAVALISSE is a kinase inhibitor indicated for the treatment of thrombocytopenia in adult patients with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment.

— FDA label: Tavalisse, Rigel Pharmaceuticals, Inc., effective November 5, 2025. 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 formsTablet
RouteOral
Prescription products2 in the FDA NDC Directory
Brand namesTavalisse

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.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA209299
TAVALISSE
Rigel PharmsApril 17, 2018 1, latest February 4, 2025
2025: Labeling

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)2044922, 2044928, 2044930, 2044932
SPL set ID of the quoted label21149cc3-049b-43e2-b141-c9499160556c
FDA labels (SPL)1
FDA applicationsNDA209299
Active ingredients (FDA)FOSTAMATINIB

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Tavalisse, Rigel Pharmaceuticals, Inc., effective November 5, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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 →

Report an error → · Information for medicine makers