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IMJUDO 20 MG — DIN 02541009

TREMELIMUMAB : 20 MG · ASTRAZENECA CANADA INC · SOLUTION · wholesale supply in Canada

Health Canada status: MARKETED

What is IMJUDO?

IMJUDO 20 MG contains TREMELIMUMAB : 20 MG. It is listed in the Health Canada Drug Product Database under DIN 02541009, held by ASTRAZENECA CANADA INC, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 23-Oct-2023. 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 IMJUDO used for?

In combination with durvalumab for the first-line treatment of adult patients with unresectable hepatocellular carcinoma (uHCC) who require systemic therapy.

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

How much does Tremelimumab cost around the world?

Tremelimumab is listed on 9 of the national price registers Nexara ingests. Each country publishes on a different basis, so those figures are not comparable with one another — or with a Canadian wholesale price.

What a market publishes matters more than the number it publishes. Australia publishes a ex-manufacturer; Bahrain publishes a retail (max); Greece publishes a producer price (ex-factory). Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.

MarketPrice basis published thereBrandsPacks listedRange
United Arab Emiratespublic22AED███.██
Australiaex-manufacturer12AUD███.██
Bahrainretail (max)12BHD███.██
Greeceproducer price (ex-factory)22EUR███.██
Italyex-factory (classe H)22EUR███.██
Norwaymax AUP (pharmacy retail)12NOK███.██
Saudi Arabiapublic12SAR███.██
Hungaryproducer price (ex-factory)11HUF███.██
Romaniamax producer price11RON███.██

16 pack listings across 12 brand entries and 7 price bases, refreshed 08 Sep 2026. Ranges span every Tremelimumab pack in that market, so a high figure is usually a larger pack rather than the same product.

Figures are held for the Nexara team. Cross-market prices are published on incompatible bases and are not an offer, a landed cost, or a guide to what any buyer can obtain. Nexara publishes which markets list the product and on what basis; the numbers stay internal.

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Canada publishes no comparable public list price. For a delivered Canadian price on a licensed account, verify your licence — it takes about a minute.

Ask Nexara for a landed Canadian price

How is it supplied and stored?

Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.

Strength on the label20 MG
Dosage formSOLUTION
RouteINTRAVENOUS
Pack configuration (monograph)1.25 mL (25 mg) or 15 mL (300 mg) concentrate in a Type I glass vial. Pack size of 1 single-dose vial.
StorageStore in a refrigerator (2°C to 8°C). Do not freeze. Store in original package to protect from light.
Shipping classCold chain — validated shipper with temperature monitoring

Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation.

Cold chain. This product is stored refrigerated. Nexara ships it on a validated cold chain with temperature monitoring; a delivery address that cannot receive and store it at 2–8 °C on arrival must be flagged before the order is placed.

Substance and classification

Active substanceTremelimumab
ATC codeL01FX20
Biosimilar biologicNo

Confirm the pack and get a price

Health Canada record and identifiers

The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.

DIN (8-digit, as used in ordering)02541009
DIN (unpadded, as printed on some documents)2541009
Brand nameIMJUDO
Generic / active ingredientTREMELIMUMAB : 20 MG
Market authorization holderASTRAZENECA CANADA INC
Health Canada schedulePrescription
ATC codeL01FX20
ATC anatomical main groupL — Antineoplastic and immunomodulating agents
ATC therapeutic subgroupL01FX
Current statusMARKETED
Status date23-Oct-2023
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

How is it administered?

300 mg as a single dose, followed by durvalumab 1500 mg at Day 1 of Cycle 1. Administer via IV infusion over 60 minutes. Weight-based dosing for patients ≤ 30 kg.

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

Contraindications

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

Warnings and precautions

Can cause severe and fatal immune-mediated adverse reactions (pneumonitis, hepatitis, colitis, endocrinopathies, nephritis, rash, myocarditis, etc.). Monitor patients continuously.

What can be used instead?

Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.

2 · Same class — other molecules in ATC L01FX

MoleculeCanadian brandsDINsMarketedSourceable
Polatuzumab VedotinPOLIVY22Yes
TeclistamabTECVAYLI22Yes
Belantamab MafodotinBLENREP22Yes
GlofitamabCOLUMVI22Yes
TalquetamabTALVEY22Yes
TarlatamabIMDELLTRA22Yes
ElranatamabELREXFIO22Yes
Enfortumab VedotinPADCEV22Yes
EpcoritamabEPKINLY22Yes
BlinatumomabBLINCYTO11Yes

A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.

3 · Adjacent classes in ATC L01F

ATC subgroupMoleculesDINsMarketed
L01FDPertuzumab · Trastuzumab · Trastuzumab Deruxtecan · Trastuzumab Emtansine1816
L01FGBevacizumab · Ramucirumab1414
L01FFAtezolizumab · Avelumab · Cemiplimab · Dostarlimab · Durvalumab · +3 more1412
L01FAObinutuzumab · Ofatumumab · Rituximab118
L01FCDaratumumab · Isatuximab55
L01FYNivolumab And Relatlimab · Pertuzumab And Trastuzumab44
L01FECetuximab · Necitumumab · Panitumumab53
L01FBInotuzumab Ozogamicin11

Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.

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.

Request a quote for IMJUDO

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. Patients and unlicensed buyers are routed to a partner pharmacy.

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.

Why is there no price on this page?

Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.

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.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database and the approved product monograph (PDF). Health Canada status reconciled against the live DPD sync. Last reviewed 10 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 02541009. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.