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HALAVEN 0.5 MG

ERIBULIN MESYLATE : 0.5 MG · DIN 02377438 · EISAI LIMITED

Health Canada status: MARKETED

What is HALAVEN?

HALAVEN 0.5 MG contains ERIBULIN MESYLATE : 0.5 MG. It is listed in the Health Canada Drug Product Database under DIN 02377438, held by EISAI LIMITED, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 19-Mar-2012. 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 HALAVEN used for?

Metastatic breast cancer (after 2+ chemo regimens including anthracycline and taxane) and unresectable advanced or metastatic liposarcoma (after anthracycline regimen).

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

DIN02377438
Brand nameHALAVEN
Generic / active ingredientERIBULIN MESYLATE : 0.5 MG
ManufacturerEISAI LIMITED
Strength0.5 MG
Dosage formSOLUTION
Route of administrationINTRAVENOUS
SchedulePrescription
ATC codeL01XX41 ERIBULIN
AHFS class10:00.00
BiosimilarNo
Health Canada statusMARKETED
Status date19-Mar-2012
Original market date2012-03-19 00:00:00

How is it administered?

1.4 mg/m2 administered intravenously over 2 to 5 minutes on Days 1 and 8 of a 21-day cycle. Dose reductions required for hepatic/renal impairment and certain toxicities.

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

How is it stored and handled?

Not explicitly detailed in the provided text (refers to Storage and Stability section).

How is it supplied?

Not explicitly detailed in the provided text (refers to Dosage Forms, Composition and Packaging section).

Contraindications

History of hypersensitivity to HALAVEN or halichondrin B or its chemical derivatives.

Warnings and precautions

Serious warnings: Neutropenia, QT/QTc interval prolongation. Monitor CBC and electrolytes. Risk of peripheral neuropathy. Avoid in severe hepatic/renal impairment.

What can be used instead?

Other Canadian products sharing ATC code L01XX41 ERIBULIN. 2 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
ERIBULIN MESYLATE INJECTION0.5 MGSOLUTIONDR REDDY'S LABORATORIES LTDMARKETEDDIN 02545950
NAT-ERIBULIN0.5 MGSOLUTIONNATCO PHARMA (CANADA) INCDORMANTDIN 02539136

Who else supplies ERIBULIN worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. ERIBULIN appears in 28 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 02377438. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.