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OJJAARA 150 MG

MOMELOTINIB (MOMELOTINIB DIHYDROCHLORIDE) : 150 MG · DIN 02552973 · GLAXOSMITHKLINE INC

Health Canada status: MARKETED

What is OJJAARA?

OJJAARA 150 MG contains MOMELOTINIB (MOMELOTINIB DIHYDROCHLORIDE) : 150 MG. It is listed in the Health Canada Drug Product Database under DIN 02552973, held by GLAXOSMITHKLINE INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 21-Jan-2025. 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 OJJAARA used for?

Treatment of splenomegaly and/or disease-related symptoms in adults with intermediate or high-risk primary, post polycythemia vera, or post essential thrombocythemia myelofibrosis with anemia.

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

DIN02552973
Brand nameOJJAARA
Generic / active ingredientMOMELOTINIB (MOMELOTINIB DIHYDROCHLORIDE) : 150 MG
ManufacturerGLAXOSMITHKLINE INC
Strength150 MG
Dosage formTABLET
Route of administrationORAL
SchedulePrescription
ATC codeL01EJ04 MOMELOTINIB
BiosimilarNo
Health Canada statusMARKETED
Status date21-Jan-2025

How is it administered?

Recommended dosage is 200 mg orally once daily. Can be taken with or without food. Tablets must be swallowed whole; do not cut, break, dissolve, crush, or chew.

Included because it drives pack selection and wastage. Consult the monograph.

How is it stored and handled?

Not explicitly detailed in the provided text snippet (section 11 is listed in TOC but content is missing).

How is it supplied?

100 mg, 150 mg, and 200 mg tablets (specific bottle/blister counts not provided in text, but descriptions of tablet appearance for each strength are included).

Contraindications

Hypersensitivity to this drug or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container.

Warnings and precautions

Serious bacterial and viral infections (some fatal). Risk of secondary malignancies, thrombosis, MACE, thrombocytopenia, neutropenia, and hepatotoxicity. Contains lactose.

What can be used instead?

Other Canadian products sharing ATC code L01EJ04 MOMELOTINIB. 3 of 3 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.

ProductStrengthFormManufacturerHealth Canada statusDIN
OJJAARA100 MGTABLETGLAXOSMITHKLINE INCMARKETEDDIN 02552965
OJJAARA200 MGTABLETGLAXOSMITHKLINE INCMARKETEDDIN 02552981

Who else supplies MOMELOTINIB worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. MOMELOTINIB appears in 27 registered pack listings across 8 markets, published on 7 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 02552973. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.