NORDIMET 15 MG / 0.6 ML — DIN 02546574
METHOTREXATE (METHOTREXATE SODIUM) : 15 MG / 0.6 ML · NORDIC GROUP B.V. · SOLUTION · wholesale supply in Canada
Health Canada status: CANCELLED POST MARKET
What is NORDIMET?
NORDIMET 15 MG / 0.6 ML contains METHOTREXATE (METHOTREXATE SODIUM) : 15 MG / 0.6 ML. It is listed in the Health Canada Drug Product Database under DIN 02546574, held by NORDIC GROUP B.V., supplied as SOLUTION for SUBCUTANEOUS administration. Health Canada currently lists it as cancelled post market, status dated 13-Mar-2026. This Drug Identification Number is no longer authorized for sale in Canada, so Nexara does not supply it. The record is kept here because buyers still meet the number on old formularies, purchase orders and tender documents; Nexara can help identify an authorized alternative.
What is NORDIMET used for?
NORDIMET (methotrexate injection) is indicated as a Disease Modifying Antirheumatic Drug (DMARD) in severe disabling active rheumatoid arthritis (RA) in adult patients and severe disabling psoriasis/psoriatic arthritis in adult patients. In psoriasis, it is restricted to severe, recalcitrant, disabling cases in adults unresponsive to other therapies, and only after dermatologic consultation and diagnosis.
Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.
How much does Methotrexate cost around the world?
Methotrexate is listed on 12 of the national price registers Nexara ingests. Each country publishes on a different basis, so those figures are not comparable with one another — or with a Canadian wholesale price.
What a market publishes matters more than the number it publishes. Australia publishes a ex-manufacturer; Austria publishes a KVP (Kassenverkaufspreis); Bahrain publishes a retail (max). Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.
| Market | Price basis published there | Brands | Packs listed | Range |
|---|---|---|---|---|
| Czechia | max producer price (ex-factory) | 9 | 77 | CZK███.██ |
| Australia | ex-manufacturer | 7 | 36 | AUD███.██ |
| Saudi Arabia | public | 19 | 33 | SAR███.██ |
| United States | acquisition | 3 | 27 | USD███.██ |
| Greece | producer price (ex-factory) | 23 | 23 | EUR███.██ |
| Austria | KVP (Kassenverkaufspreis) | 22 | 22 | EUR███.██ |
| Morocco | PPV (public price) | 8 | 17 | MAD███.██ |
| United Kingdom | hospital | 9 | 9 | GBP███.██ |
| Luxembourg | reimbursement | 9 | 9 | EUR███.██ |
| South Africa | single exit price | 7 | 7 | ZAR███.██ |
| Bahrain | retail (max) | 2 | 2 | BHD███.██ |
| United Arab Emirates | public | 1 | 1 | AED███.██ |
263 pack listings across 119 brand entries and 11 price bases, refreshed 08 Sep 2026. Ranges span every Methotrexate pack in that market, so a high figure is usually a larger pack rather than the same product.
This table is a regulatory record of where the molecule is listed. The DIN on this page is no longer authorized for sale in Canada, so Nexara does not quote it — see the alternatives above.
Is there a generic Methotrexate in Canada, and who makes it?
Every market authorization holder with a Canadian DIN for this molecule, and how many of their listings Health Canada currently shows as marketed.
6 holders have a Canadian DIN containing Methotrexate, across 41 DINs, of which 29 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.
| Market authorization holder | DINs | Marketed | Brand names | Position |
|---|---|---|---|---|
| ACCORD HEALTHCARE INC | 16 | 14 | METHOFILL SELF-DOSE INJECTOR, METHOTREXATE SUBCUTANEOUS | Sourceable in Canada |
| MEDEXUS PHARMACEUTICALS INC. | 8 | 7 | METOJECT SUBCUTANEOUS | Sourceable in Canada |
| PHARMASCIENCE INC | 7 | 7 | PMS-METHOTREXATE INJECTION | Sourceable in Canada |
| AURO PHARMA INC | 1 | 1 | AURO-METHOTREXATE | Sourceable in Canada |
| NORDIC GROUP B.V. | 8 | 0 | NORDIMET | No marketed DIN |
| WYETH-AYERST CANADA INC. | 1 | 0 | RHEUMATREX-TAB 2.5MG | No marketed DIN |
Health Canada’s Drug Product Database does not flag which listing is the originator and which are subsequent-entry products, so Nexara does not label them here. Interchangeability is determined provincially, not federally — confirm for your province before a formulary switch. Nexara can confirm which of these is actually obtainable, and on what lead time, per order.
How is it supplied and stored?
Pack configuration, storage class and the handling constraints that drive cold-chain planning. One DIN can cover more than one pack size, and the pack — not the DIN — is what gets priced, shipped and invoiced.
| Strength on the label | 15 MG / 0.6 ML |
|---|---|
| Dosage form | SOLUTION |
| Route | SUBCUTANEOUS |
| Pack configuration (monograph) | • 1 pre-filled autoinjector pen with 0.3 ml solution, containing 7.5 mg methotrexate ( beige grey) • 1 pre-filled autoinjector pen with 0.4 ml solution, containing 10.0 mg methotrexate ( light green) • 1 pre-filled autoinjector pen with 0.5 ml solution, containing 12.5 mg methotrexate ( light blue ) • 1 pre-filled autoinjector pen with 0.6 ml solution, containing 15.0 mg methotrexate (purple) • 1 pre-filled autoinjector pen with 0.7 ml solution, containing 17.5 mg methotrexate ( pink ) • 1 pre-filled autoinjector pen with 0.8 ml solution, containing 20.0 mg methotrexate (red) • 1 pre-filled autoinjector pen with 0.9 ml solution, containing 22.5 mg methotrexate (dark green) • 1 pre-filled autoinjector pen with 1.0 ml solution, containing 25.0 mg methotrexate (yellow) All strengths are separately available as a pack containing 1 pre-filled autoinjector pen and one alcohol swab, and as multipack cartons containing 4 pre-filled autoinjector pens and 4 alcohol swabs. |
| Storage | null |
Pack detail is kept as a regulatory record. This DIN is no longer authorized for sale in Canada, so Nexara does not quote this pack.
Substance and classification
| Active substance | Methotrexate |
|---|---|
| ATC code | L04AX03 |
| Biosimilar biologic | No |
Health Canada record and identifiers
The regulatory facts straight from the Drug Product Database, plus every identifier form Nexara accepts on a purchase order. A DIN written without its leading zeros is the commonest reason an order line fails to match.
| DIN (8-digit, as used in ordering) | 02546574 |
|---|---|
| DIN (unpadded, as printed on some documents) | 2546574 |
| Brand name | NORDIMET |
| Generic / active ingredient | METHOTREXATE (METHOTREXATE SODIUM) : 15 MG / 0.6 ML |
| Market authorization holder | NORDIC GROUP B.V. |
| Health Canada schedule | Prescription |
| ATC code | L04AX03 |
| ATC anatomical main group | L — Antineoplastic and immunomodulating agents |
| ATC therapeutic subgroup | L04AX |
| Current status | CANCELLED POST MARKET |
| Status date | 13-Mar-2026 |
| Status source | Live Health Canada DPD sync |
Verify on the primary sources
Is Methotrexate in shortage in Canada?
A Canadian shortage report is on file for a product containing this molecule: Resolved — reported by ACCORD HEALTHCARE INC, last seen 04 Sep 2026. A shortage on one presentation does not always affect every DIN of the molecule — the alternatives below list what else is marketed in Canada. Nexara can confirm current availability and identify substitutions or import options where permitted.
What can be used instead?
Alternatives on every axis a buyer actually considers — the same molecule in another presentation, the same class, an adjacent class, or a fixed-dose combination. Every row is led by the marketed DIN count, because that is what can be bought this week.
1 · Same molecule, other Canadian presentations
29 of 41 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.
| Product | Strength | Form | Holder | Health Canada status | DIN |
|---|---|---|---|---|---|
| AURO-METHOTREXATE | 2.5 MG | TABLET | AURO PHARMA INC | MARKETED | 02524023 |
| METHOFILL SELF-DOSE INJECTOR | 20 MG / 0.4 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530813 |
| METHOFILL SELF-DOSE INJECTOR | 17.5 MG / 0.35 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530805 |
| METHOFILL SELF-DOSE INJECTOR | 22.5 MG / 0.45 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530848 |
| METHOFILL SELF-DOSE INJECTOR | 10 MG / 0.2 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530775 |
| METHOFILL SELF-DOSE INJECTOR | 25 MG / 0.5 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530856 |
| METHOFILL SELF-DOSE INJECTOR | 12.5 MG / 0.25 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530783 |
| METHOFILL SELF-DOSE INJECTOR | 15 MG / 0.3 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02530791 |
| METHOTREXATE SUBCUTANEOUS | 25 MG / 0.5 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02491362 |
| METHOTREXATE SUBCUTANEOUS | 10 MG / 0.2 ML | SOLUTION | ACCORD HEALTHCARE INC | MARKETED | 02491281 |
2 · Same class — other molecules in ATC L04AX
| Molecule | Canadian brands | DINs | Marketed | Sourceable |
|---|---|---|---|---|
| Lenalidomide | APO-LENALIDOMIDE · EUGIA-LENALIDOMIDE · JAMP LENALIDOMIDE · LENALIDOMIDE · +6 more | 62 | 42 | Yes |
| Methotrexate | AURO-METHOTREXATE · METHOFILL SELF-DOSE INJECTOR · METHOTREXATE SUBCUTANEOUS · METOJECT SUBCUTANEOUS · +3 more | 41 | 29 | Yes |
| Pomalidomide | APO-POMALIDOMIDE · JAMP POMALIDOMIDE · NAT-POMALIDOMIDE · POMALIDOMIDE · +3 more | 28 | 24 | Yes |
| Dimethyl Fumarate | ACH-DIMETHYL FUMARATE · APO-DIMETHYL FUMARATE · AURO-DIMETHYL FUMARATE · GLN-DIMETHYL FUMARATE · +7 more | 22 | 12 | Yes |
| Pirfenidone | AURO-PIRFENIDONE · ESBRIET · JAMP PIRFENIDONE · M-PIRFENIDONE · +5 more | 19 | 12 | Yes |
| Azathioprine | APO-AZATHIOPRINE · AZATHIOPRINE · AZATHIOPRINE SODIUM FOR INJECTION · AZATHIOPRINE-50 · +8 more | 14 | 3 | Yes |
| Thalidomide | THALOMID | 4 | 2 | Yes |
| Other Immunosuppressants | PROCHYMAL | 1 | 0 | Not in Canada |
A molecule with zero marketed DINs cannot be sourced domestically, however many approvals it holds — if one of these sits on a formulary or in an older protocol, that is the line to check.
3 · Adjacent classes in ATC L04A
| ATC subgroup | Molecules | DINs | Marketed |
|---|---|---|---|
| L04AC | Anakinra · Basiliximab · Bimekizumab · Brodalumab · Canakinumab · +13 more | 85 | 75 |
| L04AB | Adalimumab · Certolizumab Pegol · Etanercept · Golimumab · Infliximab | 71 | 55 |
| L04AA | Abatacept · Alefacept · Antilymphocyte Immunoglobulin (Horse) · Antithymocyte Immunoglobulin (Rabbit) · Apremilast · +4 more | 73 | 42 |
| L04AD | Ciclosporin · Tacrolimus | 49 | 30 |
| L04AK | Leflunomide · Teriflunomide | 44 | 25 |
| L04AH | Everolimus · Sirolimus | 36 | 23 |
| L04AF | Baricitinib · Deucravacitinib · Ritlecitinib · Tofacitinib · Upadacitinib | 23 | 19 |
| L04AG | Alemtuzumab · Anifrolumab · Belimumab · Efalizumab · Inebilizumab · +7 more | 20 | 15 |
Not clinical advice. These tables describe what can be supplied in Canada, not what should be prescribed. Substitution within or across classes is a prescriber and pharmacist decision, and interchangeability is determined provincially.
What else is NORDIMET called?
The same molecule, Methotrexate, is registered under other names elsewhere. Buyers and prescribers searching from outside Canada — or working from a foreign prescription or tender document — often know it by one of these:
| Name | Script | Registered in |
|---|---|---|
| METOJECT PEN | Latin | Czechia |
| INJEXATE | Latin | Czechia |
| TREXAN NEO | Latin | Czechia |
| Trexject | Latin | Australia |
| DBL Methotrexate | Latin | Australia |
| INJEXATE AUTOINJEKTOR | Latin | Czechia |
| Metoject | Latin | Czechia, Saudi Arabia |
| FOXIEMO | Latin | Czechia |
| Chexate | Latin | Australia |
| Methoblastin | Latin | Australia |
| METHOTREXAT EBEWE | Latin | Czechia |
| Methotrexate Accord | Latin | Australia |
| METHOTREXATE BIODIM | Latin | Morocco |
| Methotrexate Ebewe | Latin | Australia |
| ARX-Methotrexate | Latin | Australia |
Names are taken from national medicine registers and published price lists. A product registered abroad is not authorized for sale in Canada unless it holds its own DIN; import is possible only through the routes Health Canada permits.
Can this still be bought in Canada?
No. This Drug Identification Number is cancelled post market in Health Canada's Drug Product Database, so the product is no longer authorized for sale in Canada and Nexara does not supply it. This page is kept as a regulatory record.
If you are looking for a current equivalent, the alternatives above list every product sharing this therapeutic class, with the marketed ones first. Ask us to source an alternative
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. Patients and unlicensed buyers are routed to a partner pharmacy.
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.
Why is there no price on this page?
Nexara quotes a delivered Canadian price per order, against a verified licence. Foreign list prices are published on incompatible bases and are not a guide to what any buyer can obtain here, so this page shows which markets list the molecule and on what basis, and nothing more.
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.