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KINLYTIC OPEN-CATH 5000 UNIT

UROKINASE : 5000 UNIT · DIN 00886777 · MICROBIX BIOSYSTEMS INC

Health Canada status: CANCELLED POST MARKET

What is KINLYTIC OPEN-CATH?

KINLYTIC OPEN-CATH 5000 UNIT contains UROKINASE : 5000 UNIT. It is listed in the Health Canada Drug Product Database under DIN 00886777, held by MICROBIX BIOSYSTEMS INC, supplied as POWDER FOR SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as cancelled post market, status dated 28-Oct-2009. 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 KINLYTIC OPEN-CATH used for?

KINLYTIC® OPEN-CATH® (urokinase for catheter clearance) is indicated for the restoration of patency to intravenous catheters, including central venous catheters, obstructed by clotted blood or fibrin.

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

DIN00886777
Brand nameKINLYTIC OPEN-CATH
Generic / active ingredientUROKINASE : 5000 UNIT
ManufacturerMICROBIX BIOSYSTEMS INC
Strength5000 UNIT
Dosage formPOWDER FOR SOLUTION
Route of administrationINTRAVENOUS
ScheduleSchedule D
ATC codeB01AD04 UROKINASE
AHFS class20:12.20
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date28-Oct-2009
Original market date1991-12-31 00:00:00

How is it administered?

Instill 1 mL or 1.8 mL (5000 IU/mL) into occluded catheter. Wait 5-30 mins, then aspirate. May repeat if necessary. Aspirate 4-5 mL blood after patency restored to remove drug/clot residue.

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

How is it stored and handled?

Store powder below 25°C. Avoid freezing.

How is it supplied?

5,000 IU DIL-U-VIAL* (1 mL when mixed with diluent in upper chamber) and 9,000 IU DIL-U-VIAL* (1.8 mL when mixed with diluent in upper chamber) providing 5,000 IU of urokinase activity per mL

Contraindications

Hypersensitivity to urokinase; active internal bleeding, history of CVA, recent intracranial/intraspinal surgery, recent trauma, intracranial neoplasm, severe hypertension, aortic dissection.

Warnings and precautions

Potential risk of transmitting infectious agents (human cell source). Avoid excessive pressure during injection to prevent catheter rupture or clot expulsion. Not effective for non-fibrin occlusions.

What can be used instead?

Other Canadian products sharing ATC code B01AD04 UROKINASE. 0 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
KINLYTIC (UROKINASE FOR INJECTION)250000 UNITPOWDER FOR SOLUTIONMICROBIX BIOSYSTEMS INCCANCELLED POST MARKETDIN 00749702

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 KINLYTIC OPEN-CATH

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 00886777. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.