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RYDAPT 25 MG

MIDOSTAURIN : 25 MG · DIN 02466236 · NOVARTIS PHARMACEUTICALS CANADA INC

Health Canada status: MARKETED

What is RYDAPT?

RYDAPT 25 MG contains MIDOSTAURIN : 25 MG. It is listed in the Health Canada Drug Product Database under DIN 02466236, held by NOVARTIS PHARMACEUTICALS CANADA INC, supplied as CAPSULE for ORAL administration. Health Canada currently lists it as marketed, status dated 08-Sep-2017. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.

What is RYDAPT used for?

RYDAPT is indicated in combination with standard cytarabine and daunorubicin induction and cytarabine consolidation chemotherapy for the treatment of adult patients with newly diagnosed FLT3-mutated acute myeloid leukemia (AML). RYDAPT is indicated for the treatment of adult patients with aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated hematological neoplasm (SM-AHN), or mast cell leukemia (MCL).

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

Product details and regulatory record

DIN02466236
Brand nameRYDAPT
Generic / active ingredientMIDOSTAURIN : 25 MG
ManufacturerNOVARTIS PHARMACEUTICALS CANADA INC
Strength25 MG
Dosage formCAPSULE
Route of administrationORAL
SchedulePrescription
ATC codeL01EX10 MIDOSTAURIN
AHFS class10:00.00
BiosimilarNo
Health Canada statusMARKETED
Status date08-Sep-2017
Original market date2017-09-08 00:00:00

How is it stored and handled?

null

How is it supplied?

blisters, in multipacks of 56 and 112 capsules.

Who else supplies MIDOSTAURIN worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. MIDOSTAURIN appears in 18 registered pack listings across 10 markets, published on 8 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.

Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

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Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

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Health Canada Drug Product Database (DPD), DIN 02466236. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.