Quick answers
- What is Rydapt used for?
- The FDA-approved label (Rydapt, Novartis Pharmaceuticals Corporation, June 8, 2026) says: “RYDAPT is a kinase inhibitor indicated for the treatment of adult patients with: Newly diagnosed acute myeloid leukemia (AML) that is FLT3 mutation-positive as detected by an FDA-approved test, in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation. Limitations of Use: RYDAPT is not indicated as a single-agent induction therapy for the treatment of patients with AML. …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Rydapt 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 Rydapt?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Rydapt been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Rydapt?
- 1 company lists prescription products of Rydapt in the FDA NDC Directory, including Novartis Pharmaceuticals Corporation.
What Rydapt is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
RYDAPT is a kinase inhibitor indicated for the treatment of adult patients with: Newly diagnosed acute myeloid leukemia (AML) that is FLT3 mutation-positive as detected by an FDA-approved test, in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation. Limitations of Use: RYDAPT is not indicated as a single-agent induction therapy for the treatment of patients with AML. …
— FDA label: Rydapt, Novartis Pharmaceuticals Corporation, effective June 8, 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.
Conditions named on the label
These condition names appear word for word in the label’s “Indications and Usage” text (matched with a reviewed table). Each page lists hospitals whose own websites name the condition.
Related medical specialties
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, liquid filled |
|---|---|
| Route | Oral |
| Prescription products | 1 in the FDA NDC Directory |
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.
- Novartis Pharmaceuticals Corporation1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA207997 RYDAPT | Novartis | April 28, 2017 | 6, latest May 22, 2023 2023: Labeling · 2021: Labeling · 2021: 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) | 1919088 |
|---|---|
| SPL set ID of the quoted label | 11fa3fc9-6776-49a6-b1c1-653f627c3e58 |
| FDA labels (SPL) | 1 |
| FDA applications | NDA207997 |
| Active ingredients (FDA) | MIDOSTAURIN |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Rydapt, Novartis Pharmaceuticals Corporation, effective June 8, 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 →