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BERIPLEX P/N 1000 1240 UNIT — DIN 02410826

COAGULATION FACTOR IX (HUMAN) : 1240 UNIT COAGULATION FACTOR II (HUMAN) : 1600 UNIT COAGULATION FACTOR VII (HUMAN) : 1000 UNIT PROTEIN S : 1360 UNIT PROTEIN C : 1640 UNIT COAGULATION FACTOR X (HUMAN) : 2040 UNIT · CSL BEHRING CANADA INC · POWDER FOR SOLUTION · wholesale supply in Canada

Health Canada status: MARKETED

What is BERIPLEX P/N 1000?

BERIPLEX P/N 1000 1240 UNIT contains COAGULATION FACTOR IX (HUMAN) : 1240 UNIT COAGULATION FACTOR II (HUMAN) : 1600 UNIT COAGULATION FACTOR VII (HUMAN) : 1000 UNIT PROTEIN S : 1360 UNIT PROTEIN C : 1640 UNIT COAGULATION FACTOR X (HUMAN) : 2040 UNIT. It is listed in the Health Canada Drug Product Database under DIN 02410826, held by CSL BEHRING CANADA INC, supplied as POWDER FOR SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 21-Nov-2013. 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 BERIPLEX P/N 1000 used for?

Beriplex® P/N (Human prothrombin complex) is indicated in adults (≥ 18 years of age) for the treatment of bleeding and perioperative prophylaxis of bleeding in acquired deficiency of the prothrombin complex coagulation factors, such as deficiency caused by treatment with vitamin K antagonists, or in case of overdose of vitamin K antagonists, when rapid correction of the deficiency is required. Beriplex® P/N can be used for the treatment of bleeding and perioperative prophylaxis of bleeding in congenital deficiency of any of the vitamin K dependent coagulation factors only if purified specific coagulation factor product is not available.

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 Coagulation Factor Ix, Ii, Vii And X 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.

2 holders have a Canadian DIN containing Coagulation Factor Ix, Ii, Vii And X In Comb, across 4 DINs, of which 4 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 INC22BERIPLEX P/N 1000, BERIPLEX P/N 500Sourceable in Canada
OCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B H22OCTAPLEXSourceable in Canada

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 label1240 UNIT
Dosage formPOWDER FOR SOLUTION
RouteINTRAVENOUS
Pack configuration (monograph)Beriplex ® P/N 500: 500 IU Factor IX/vial with 20 mL solvent; Beriplex ® P/N 1000: 1000 IU factor IX/vial with 40 mL solvent. Each package includes a needle-less filter transfer device Mix2Vial®.
StorageSee section 11 Storage, Stability, and Disposal for the recommended storage period and conditions. If not administered immediately, storage shall not exceed 3 hours at room temperature.

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

Substance and classification

Active substanceCoagulation Factor Ix, Ii, Vii And X In Comb
ATC codeB02BD01
AHFS class28:16.04.20
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)02410826
DIN (unpadded, as printed on some documents)2410826
Brand nameBERIPLEX P/N 1000
Generic / active ingredientCOAGULATION FACTOR IX (HUMAN) : 1240 UNIT COAGULATION FACTOR II (HUMAN) : 1600 UNIT COAGULATION FACTOR VII (HUMAN) : 1000 UNIT PROTEIN S : 1360 UNIT PROTEIN C : 1640 UNIT COAGULATION FACTOR X (HUMAN) : 2040 UNIT
Market authorization holderCSL BEHRING CANADA INC
Health Canada scheduleSchedule D
ATC codeB02BD01
ATC anatomical main groupB — Blood and blood-forming organs
ATC therapeutic subgroupB02BD
Current statusMARKETED
Status date21-Nov-2013
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

How is it administered?

Individualized dose based on INR and body weight (up to 100kg). Administer IV at max 3 IU/kg/min (max 210 IU/min). Administer Vitamin K concurrently.

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

Contraindications

Hypersensitivity to active substance or excipients; disseminated intravascular coagulation (until consumptive state ends); known history of heparin-induced thrombocytopenia.

Warnings and precautions

Risk of thrombosis and DIC. Monitor for thromboembolic events. Risk of transmitting infectious agents (human plasma-derived). Contains heparin (risk of HIT).

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

4 of 4 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
BERIPLEX P/N 500680 UNITPOWDER FOR SOLUTIONCSL BEHRING CANADA INCMARKETED02359251
OCTAPLEX480 UNITKIT ; POWDER FOR SOLUTIONOCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B HMARKETED02294664
OCTAPLEX1240 UNITPOWDER FOR SOLUTION ; KITOCTAPHARMA PHARMAZEUTIKA PRODUKTIONSGES M B HMARKETED02434970

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.

Request a quote for BERIPLEX P/N 1000

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 02410826. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.