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PROBUPHINE 80 MG

BUPRENORPHINE HYDROCHLORIDE : 80 MG · DIN 02474921 · KNIGHT THERAPEUTICS INC.

Health Canada status: CANCELLED POST MARKET

What is PROBUPHINE?

PROBUPHINE 80 MG contains BUPRENORPHINE HYDROCHLORIDE : 80 MG. It is listed in the Health Canada Drug Product Database under DIN 02474921, held by KNIGHT THERAPEUTICS INC., supplied as IMPLANT for SUBCUTANEOUS administration. Health Canada currently lists it as cancelled post market, status dated 30-Jun-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

DIN02474921
Brand namePROBUPHINE
Generic / active ingredientBUPRENORPHINE HYDROCHLORIDE : 80 MG
ManufacturerKNIGHT THERAPEUTICS INC.
Strength80 MG
Dosage formIMPLANT
Route of administrationSUBCUTANEOUS
ScheduleNARCOTICS (CDSA I)
ATC codeN07BC01 BUPRENORPHINE
AHFS class28:08.12
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date30-Jun-2023
Original market date2018-11-22 00:00:00

What can be used instead?

Other Canadian products sharing ATC code N07BC01 BUPRENORPHINE. 2 of 3 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
SUBLOCADE100 MG / 0.5 MLSOLUTION (EXTENDED RELEASE)INDIVIOR UK LIMITEDMARKETEDDIN 02483084
SUBLOCADE300 MG / 1.5 MLSOLUTION (EXTENDED RELEASE)INDIVIOR UK LIMITEDMARKETEDDIN 02483092

Who else supplies BUPRENORPHINE worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. BUPRENORPHINE appears in 392 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 02474921. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.