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AIMOVIG 70 MG

ERENUMAB : 70 MG · DIN 02479605 · NOVARTIS PHARMACEUTICALS CANADA INC

Health Canada status: APPROVED

What is AIMOVIG?

AIMOVIG 70 MG contains ERENUMAB : 70 MG. It is listed in the Health Canada Drug Product Database under DIN 02479605, held by NOVARTIS PHARMACEUTICALS CANADA INC, supplied as SOLUTION for SUBCUTANEOUS administration. Health Canada currently lists it as approved, status dated 01-Aug-2018. 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.

Product details and regulatory record

DIN02479605
Brand nameAIMOVIG
Generic / active ingredientERENUMAB : 70 MG
ManufacturerNOVARTIS PHARMACEUTICALS CANADA INC
Strength70 MG
Dosage formSOLUTION
Route of administrationSUBCUTANEOUS
ScheduleSchedule D
ATC codeN02CD01 ERENUMAB
AHFS class28:32.12
BiosimilarNo
Health Canada statusAPPROVED
Status date01-Aug-2018

What can be used instead?

Other Canadian products sharing ATC code N02CD01 ERENUMAB. 2 of 4 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
AIMOVIG140 MGSOLUTIONNOVARTIS PHARMACEUTICALS CANADA INCMARKETEDDIN 02487306
AIMOVIG70 MGSOLUTIONNOVARTIS PHARMACEUTICALS CANADA INCMARKETEDDIN 02479613
AIMOVIG140 MGSOLUTIONNOVARTIS PHARMACEUTICALS CANADA INCAPPROVEDDIN 02487292

Who else supplies ERENUMAB worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. ERENUMAB appears in 20 registered pack listings across 10 markets, published on 9 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 02479605. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.