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WILATE 500 UNIT / 5 ML — DIN 02286750

VON WILLEBRAND FACTOR (HUMAN) : 500 UNIT / 5 ML HUMAN PLASMA PROTEINS : 7.5 MG / 5 ML ANTIHEMOPHILIC FACTOR (HUMAN) : 500 UNIT / 5 ML · OCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H · POWDER FOR SOLUTION · wholesale supply in Canada

Health Canada status: MARKETED

What is WILATE?

WILATE 500 UNIT / 5 ML contains VON WILLEBRAND FACTOR (HUMAN) : 500 UNIT / 5 ML HUMAN PLASMA PROTEINS : 7.5 MG / 5 ML ANTIHEMOPHILIC FACTOR (HUMAN) : 500 UNIT / 5 ML. It is listed in the Health Canada Drug Product Database under DIN 02286750, held by OCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H, supplied as POWDER FOR SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 29-Apr-2008. 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 WILATE used for?

wilate® is indicated for: Treatment and prophylaxis of bleeding in patients with hemophilia A (congenital or acquired FVIII deficiency) and for the prevention and treatment of bleeding in minor surgical procedures. wilate® is indicated for: Treatment and prophylaxis of spontaneous and trauma-induced bleeds in all types of VWD in adult and pediatric patients where use of DDAVP (1-deamino-8-D-arginine vasopressin/desmopressin) treatment is ineffective or contra-indicated. Prevention and treatment of bleeding during and after surgical procedures.

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

Is there a generic Von Willebrand Factor And Coag. Fact. Viii In Comb in Canada, and who makes it?

Every market authorization holder with a Canadian DIN for this molecule, and how many of their listings Health Canada currently shows as marketed.

3 holders have a Canadian DIN containing Von Willebrand Factor And Coag. Fact. Viii In Comb, across 10 DINs, of which 5 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
CSL BEHRING CANADA INC33HUMATE-PSourceable in Canada
OCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H22WILATESourceable in Canada
GRIFOLS BIOLOGICALS LLC50ALPHANATENo marketed DIN

Health Canada’s Drug Product Database does not flag which listing is the originator and which are subsequent-entry products, so Nexara does not label them here. Interchangeability is determined provincially, not federally — confirm for your province before a formulary switch. Nexara can confirm which of these is actually obtainable, and on what lead time, per order.

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 label500 UNIT / 5 ML
Dosage formPOWDER FOR SOLUTION
RouteINTRAVENOUS
Pack configuration (monograph)wilate® 500 in 5 mL, 1 package contains: 1 vial with powder, 1 vial with solvent (5 mL Water for Injection with 0.1% Polysorbate 80), 1 transfer device (Nextaro®) with integrated filter. wilate® 1000 in 10 mL, 1 package contains: 1 vial with powder, 1 vial with solvent (10 mL Water for Injection with 0.1% Polysorbate 80), 1 transfer device (Nextaro®) with integrated filter.
StorageWarm the wilate® powder and solvent in the closed vials up to room temperature (maximum +37°C).

Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation, because this listing covers more than one of them.

Substance and classification

Active substanceVon Willebrand Factor And Coag. Fact. Viii In Comb
ATC codeB02BD06
AHFS class20:28.16
Biosimilar biologicNo

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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)02286750
DIN (unpadded, as printed on some documents)2286750
Brand nameWILATE
Generic / active ingredientVON WILLEBRAND FACTOR (HUMAN) : 500 UNIT / 5 ML HUMAN PLASMA PROTEINS : 7.5 MG / 5 ML ANTIHEMOPHILIC FACTOR (HUMAN) : 500 UNIT / 5 ML
Market authorization holderOCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H
Health Canada scheduleSchedule D
ATC codeB02BD06
ATC anatomical main groupB — Blood and blood-forming organs
ATC therapeutic subgroupB02BD
Current statusMARKETED
Status date29-Apr-2008
Original market date2008-04-29 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

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.

1 · Same molecule, other Canadian presentations

5 of 10 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
HUMATE-P600 UNIT / 5 MLPOWDER FOR SOLUTIONCSL BEHRING CANADA INCMARKETED02261219
HUMATE-P1200 UNIT / 10 MLPOWDER FOR SOLUTIONCSL BEHRING CANADA INCMARKETED02261227
HUMATE-P2400 UNIT / 15 MLPOWDER FOR SOLUTIONCSL BEHRING CANADA INCMARKETED02261235
WILATE1000 UNIT / 10 MLPOWDER FOR SOLUTIONOCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B HMARKETED02286769
ALPHANATE300 UNITPOWDER FOR SOLUTIONGRIFOLS BIOLOGICALS LLCAPPROVED02475561
ALPHANATE500 UNITPOWDER FOR SOLUTIONGRIFOLS BIOLOGICALS LLCAPPROVED02475588
ALPHANATE1200 UNITPOWDER FOR SOLUTIONGRIFOLS BIOLOGICALS LLCAPPROVED02475596
ALPHANATE1500 UNITPOWDER FOR SOLUTIONGRIFOLS BIOLOGICALS LLCAPPROVED02475618
ALPHANATE2000 UNITPOWDER FOR SOLUTIONGRIFOLS BIOLOGICALS LLCAPPROVED02475626

2 · Same class — other molecules in ATC B02BD

MoleculeCanadian brandsDINsMarketedSourceable
Coagulation Factor ViiiADVATE · ADYNOVATE · AFSTYLA · ALTUVIIIO · +34 more13438Yes
Coagulation Factor IxALPHANINE PWS INJ 1500UNIT/VIAL · ALPROLIX · BEBULIN VH 500UNIT/VIAL · BEBULIN VH INJ 1000UNIT/VIAL · +8 more3316Yes
Von Willebrand Factor And Coag. Fact. Viii In CombALPHANATE · HUMATE-P · WILATE105Yes
Coagulation Factor Ix, Ii, Vii And X In CombBERIPLEX P/N 1000 · BERIPLEX P/N 500 · OCTAPLEX44Yes
Coagulation Factor ViiaNIASTASE · NIASTASE RT113Yes
Factor Viii Inhibitor Bypassing ActivityFEIBA NF · FEIBA VH IMMUNO ANTI INHIBITOR52Yes
Coagulation Factor XiiiCORIFACT 1250 · CORIFACT 25022Yes
ThrombinRECOTHROM · THROMBOGEN SPRAY KIT · VISTASEAL41Yes
CatridecacogTRETTEN11Yes
Etranacogene DezaparvovecHEMGENIX11Yes

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 B02B

ATC subgroupMoleculesDINsMarketed
B02BXAvatrombopag · Concizumab · Eltrombopag · Emicizumab · Fostamatinib · +1 more2315
B02BCCombinations · Epinephrine · Local Hemostatics · Thrombin236
B02BAPhytomenadione52
B02BBFibrinogen, Human22

4 · Fixed-dose combinations with Canadian supply

ProductActive ingredientsHolderStatusDIN
ADYNOVATEANTIHEMOPHILIC FACTOR (RECOMBINANT), PEGYLATED : 1000 UNITTAKEDA CANADA INCMARKETED02498588
ALPROLIXRECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN : 500 UNITSANOFI-AVENTIS CANADA INCMARKETED02422913
ALTUVIIIO*ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC-VWF-XTEN FUSION PROTEIN : 4000 UNITSANOFI-AVENTIS CANADA INCMARKETED02448157
ELOCTATEANTIHEMOPHILIC FACTOR (RECOMBINANT BDD), FC FUSION PROTEIN : 500 UNITSANOFI-AVENTIS CANADA INCMARKETED02430304
ESPEROCTANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN TRUNCATED), PEGYLATED : 2000 UNITNOVO NORDISK CANADA INCMARKETED02490099
JIVIANTIHEMOPHILIC FACTOR (RECOMBINANT, B-DOMAIN DELETED, PEGYLATED) : 1000 UNITBAYER INCMARKETED02481774
REBINYNCOAGULATION FACTOR IX (RECOMBINANT), PEGYLATED : 3000 UNITNOVO NORDISK CANADA INCMARKETED02532964

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.

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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. 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 02286750. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.