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OPDIVO 100 MG

NIVOLUMAB : 10 MG · DIN 02446626 · BRISTOL-MYERS SQUIBB CANADA

Health Canada status: MARKETED

OPDIVO 100 MG SOLUTION - DIN 02446626
OPDIVO — DIN 02446626. Product photograph held by Nexara Health.

What is OPDIVO?

OPDIVO 100 MG contains NIVOLUMAB : 10 MG. It is listed in the Health Canada Drug Product Database under DIN 02446626, held by BRISTOL-MYERS SQUIBB CANADA, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 23-Oct-2015. 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 OPDIVO used for?

Melanoma (unresectable, metastatic, or adjuvant), NSCLC, MPM, RCC, SCCHN, cHL, MSI-H/dMMR Colorectal Cancer, Esophageal/GEJ Cancer, Gastric Cancer, Urothelial Carcinoma, HCC.

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

DIN02446626
Brand nameOPDIVO
Generic / active ingredientNIVOLUMAB : 10 MG
ManufacturerBRISTOL-MYERS SQUIBB CANADA
Strength100 MG
Dosage formSOLUTION
Route of administrationINTRAVENOUS
SchedulePrescription
ATC codeL01FF01 NIVOLUMAB
AHFS class10:00.00
BiosimilarNo
Health Canada statusMARKETED
Status date23-Oct-2015
Original market date2015-10-23 00:00:00

How is it administered?

Administered as intravenous infusion over 30 minutes. Dosages vary by indication: commonly 240 mg every 2 weeks, 480 mg every 4 weeks, or 1-3 mg/kg depending on monotherapy or combination use.

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

How is it stored and handled?

Not explicitly detailed in the provided summary text, though listed as a section in the table of contents.

How is it supplied?

40 mg and 100 mg single-use vials.

Contraindications

Hypersensitivity to nivolumab or to any ingredient in the formulation, including any non-medicinal ingredient, or component of the container.

Warnings and precautions

Severe and fatal immune-mediated adverse reactions involving any organ system. Early diagnosis and management essential. Discontinue for severe/life-threatening reactions.

What can be used instead?

Other Canadian products sharing ATC code L01FF01 NIVOLUMAB. 3 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
OPDIVO10 MGSOLUTIONBRISTOL-MYERS SQUIBB CANADAMARKETEDDIN 02446634
OPDIVO SC120 MGSOLUTIONBRISTOL-MYERS SQUIBB CANADAMARKETEDDIN 02557320

Who else supplies NIVOLUMAB worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. NIVOLUMAB appears in 38 registered pack listings across 9 markets, published on 7 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 02446626. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.