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FASTURTEC 7.5 MG

RASBURICASE : 7.5 MG · DIN 02271397 · SANOFI-AVENTIS CANADA INC

Health Canada status: CANCELLED PRE MARKET

What is FASTURTEC?

FASTURTEC 7.5 MG contains RASBURICASE : 7.5 MG. It is listed in the Health Canada Drug Product Database under DIN 02271397, held by SANOFI-AVENTIS CANADA INC, supplied as POWDER FOR SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as cancelled pre market, status dated 16-Jan-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.

Product details and regulatory record

DIN02271397
Brand nameFASTURTEC
Generic / active ingredientRASBURICASE : 7.5 MG
ManufacturerSANOFI-AVENTIS CANADA INC
Strength7.5 MG
Dosage formPOWDER FOR SOLUTION
Route of administrationINTRAVENOUS
ScheduleSchedule D
ATC codeV03AF07 RASBURICASE
AHFS class44:00.00
BiosimilarNo
Health Canada statusCANCELLED PRE MARKET
Status date16-Jan-2023

What can be used instead?

Other Canadian products sharing ATC code V03AF07 RASBURICASE. 1 of 2 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
FASTURTEC1.5 MGPOWDER FOR SOLUTIONSANOFI-AVENTIS CANADA INCMARKETEDDIN 02248416

Who else supplies RASBURICASE worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. RASBURICASE appears in 9 registered pack listings across 6 markets, published on 5 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.

Can this still be bought in Canada?

No. This Drug Identification Number is cancelled pre market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.

If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative

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.

Health Canada Drug Product Database (DPD), DIN 02271397. Last reviewed 2026-09-09. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.