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TREMFYA 200 MG / 2 ML

GUSELKUMAB : 200 MG / 2 ML · DIN 02559137 · JANSSEN INC

Health Canada status: APPROVED

What is TREMFYA?

TREMFYA 200 MG / 2 ML contains GUSELKUMAB : 200 MG / 2 ML. It is listed in the Health Canada Drug Product Database under DIN 02559137, held by JANSSEN INC, supplied as SOLUTION for SUBCUTANEOUS administration. Health Canada currently lists it as approved, status dated 07-Jul-2025. 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

DIN02559137
Brand nameTREMFYA
Generic / active ingredientGUSELKUMAB : 200 MG / 2 ML
ManufacturerJANSSEN INC
Strength200 MG / 2 ML
Dosage formSOLUTION
Route of administrationSUBCUTANEOUS
SchedulePrescription
ATC codeL04AC16 GUSELKUMAB
BiosimilarNo
Health Canada statusAPPROVED
Status date07-Jul-2025

What can be used instead?

Other Canadian products sharing ATC code L04AC16 GUSELKUMAB. 4 of 5 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
TREMFYA100 MG / 1 MLSOLUTIONJANSSEN INCMARKETEDDIN 02469758
TREMFYA200 MG / 2 MLSOLUTIONJANSSEN INCMARKETEDDIN 02559145
TREMFYA I.V.200 MG / 20 MLSOLUTIONJANSSEN INCMARKETEDDIN 02559153
TREMFYA ONE-PRESS100 MG / 1 MLSOLUTIONJANSSEN INCMARKETEDDIN 02487314

Who else supplies GUSELKUMAB worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. GUSELKUMAB appears in 43 registered pack listings across 12 markets, published on 10 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 02559137. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.