DUPIXENT 200 MG / 1.14 ML
DUPILUMAB : 200 MG / 1.14 ML · DIN 02492504 · SANOFI-AVENTIS CANADA INC
Health Canada status: MARKETED
What is DUPIXENT?
DUPIXENT 200 MG / 1.14 ML contains DUPILUMAB : 200 MG / 1.14 ML. It is listed in the Health Canada Drug Product Database under DIN 02492504, held by SANOFI-AVENTIS CANADA INC, supplied as SOLUTION for SUBCUTANEOUS administration. Health Canada currently lists it as marketed, status dated 29-Nov-2019. 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 DUPIXENT used for?
Treatment of atopic dermatitis (6m+), asthma (6y+), COPD (adults), CRSwNP (adults), eosinophilic esophagitis (1y+, 15kg+), prurigo nodularis (adults), and chronic spontaneous urticaria (12y+).
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
| DIN | 02492504 |
|---|---|
| Brand name | DUPIXENT |
| Generic / active ingredient | DUPILUMAB : 200 MG / 1.14 ML |
| Manufacturer | SANOFI-AVENTIS CANADA INC |
| Strength | 200 MG / 1.14 ML |
| Dosage form | SOLUTION |
| Route of administration | SUBCUTANEOUS |
| Schedule | Prescription |
| ATC code | D11AH05 DUPILUMAB |
| AHFS class | 84:06.28 |
| Biosimilar | No |
| Health Canada status | MARKETED |
| Status date | 29-Nov-2019 |
| Original market date | 2019-11-29 00:00:00 |
How is it administered?
Subcutaneous injection. Adults with Atopic Dermatitis: Initial 600 mg, then 300 mg Q2W. Asthma/COPD/CRSwNP/EoE/PN/CSU doses vary by age, weight, and condition. Training required for self-injection.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Not explicitly detailed in the provided text snippet (refer to section 11 of full monograph).
How is it supplied?
Packs containing 1 or 2 pre-filled syringes with needle shield or pre-filled pens. Available in 2.25 mL (300 mg) or 1.14 mL (200 mg) glass syringes.
Contraindications
Contraindicated in patients who are hypersensitive to this drug or to any ingredient in the formulation or component of the container.
Warnings and precautions
Do not use for acute asthma/COPD symptoms. Do not stop corticosteroids abruptly. Hypersensitivity reactions (anaphylaxis, serum sickness) have been reported.
What can be used instead?
Other Canadian products sharing ATC code D11AH05 DUPILUMAB. 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.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| DUPIXENT | 200 MG / 1.14 ML | SOLUTION | SANOFI-AVENTIS CANADA INC | MARKETED | DIN 02524252 |
| DUPIXENT | 300 MG / 2 ML | SOLUTION | SANOFI-AVENTIS CANADA INC | MARKETED | DIN 02470365 |
| DUPIXENT | 300 MG / 2 ML | SOLUTION | SANOFI-AVENTIS CANADA INC | MARKETED | DIN 02510049 |
| DUPIXENT | 100 MG / 0.67 ML | SOLUTION | SANOFI-AVENTIS CANADA INC | CANCELLED PRE MARKET | DIN 02526190 |
Who else supplies DUPILUMAB worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. DUPILUMAB appears in 86 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.
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.