APTIOM 600 MG — DIN 02426889
ESLICARBAZEPINE ACETATE : 600 MG · SUMITOMO PHARMA CANADA, INC. · TABLET · wholesale supply in Canada
Health Canada status: CANCELLED POST MARKET
What is APTIOM?
APTIOM 600 MG contains ESLICARBAZEPINE ACETATE : 600 MG. It is listed in the Health Canada Drug Product Database under DIN 02426889, held by SUMITOMO PHARMA CANADA, INC., supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 30-Jun-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 APTIOM used for?
Monotherapy for partial-onset seizures in adults. Adjunctive therapy for partial-onset seizures in adults and children above 6 years of age.
Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.
How much does Eslicarbazepine cost around the world?
Eslicarbazepine is listed on 2 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. Hungary publishes a producer price (ex-factory); United States publishes a acquisition. 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 |
|---|---|---|---|---|
| United States | acquisition | 4 | 28 | USD███.██ |
| Hungary | producer price (ex-factory) | 1 | 1 | HUF███.██ |
29 pack listings across 5 brand entries and 2 price bases, refreshed 03 Sep 2026. Ranges span every Eslicarbazepine pack in that market, so a high figure is usually a larger pack rather than the same product.
Canada publishes no comparable public list price. For a delivered Canadian price on a licensed account, verify your licence — it takes about a minute.
Is there a generic Eslicarbazepine 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.
3 holders have a Canadian DIN containing Eslicarbazepine, across 12 DINs, of which 8 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 |
|---|---|---|---|---|
| APOTEX INC | 4 | 4 | APO-ESLICARBAZEPINE | Sourceable in Canada |
| AURO PHARMA INC | 4 | 4 | AURO-ESLICARBAZEPINE | Sourceable in Canada |
| SUMITOMO PHARMA CANADA, INC. | 4 | 0 | APTIOM | 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 | 600 MG |
|---|---|
| Dosage form | TABLET |
| Route | ORAL |
| Pack configuration (monograph) | 200 mg, 400 mg, 600 mg and 800 mg tablets. (Specific container details not provided in text). |
| Storage | Not specified in provided text snippet. |
Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation.
Substance and classification
| Active substance | Eslicarbazepine |
|---|---|
| ATC code | N03AF04 |
| AHFS class | 28:12.92 |
| 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) | 02426889 |
|---|---|
| DIN (unpadded, as printed on some documents) | 2426889 |
| Brand name | APTIOM |
| Generic / active ingredient | ESLICARBAZEPINE ACETATE : 600 MG |
| Market authorization holder | SUMITOMO PHARMA CANADA, INC. |
| Health Canada schedule | Prescription |
| ATC code | N03AF04 |
| ATC anatomical main group | N — Nervous system |
| ATC therapeutic subgroup | N03AF |
| Current status | CANCELLED POST MARKET |
| Status date | 30-Jun-2026 |
| Original market date | 2014-08-07 00:00:00 |
| Status source | Live Health Canada DPD sync |
Verify on the primary sources
How is it administered?
Monotherapy: Adults. Adjunctive: Adults and children >6 years. Gradual withdrawal recommended. Dose adjustment required in renal impairment.
Included because it drives pack selection and wastage. Consult the monograph.
Contraindications
Hypersensitivity to eslicarbazepine acetate or other carboxamide derivatives (e.g., carbamazepine, oxcarbazepine). Patients with second- or third-degree atrioventricular (AV) block.
Warnings and precautions
Suicidal ideation/behaviour; serious dermatologic reactions (SJS/TEN); drug-induced liver injury; hyponatremia; PR interval prolongation; neurological effects (dizziness, somnolence).
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
8 of 12 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.
| Product | Strength | Form | Holder | Health Canada status | DIN |
|---|---|---|---|---|---|
| APO-ESLICARBAZEPINE | 600 MG | TABLET | APOTEX INC | MARKETED | 02537966 |
| APO-ESLICARBAZEPINE | 400 MG | TABLET | APOTEX INC | MARKETED | 02537958 |
| APO-ESLICARBAZEPINE | 800 MG | TABLET | APOTEX INC | MARKETED | 02537974 |
| APO-ESLICARBAZEPINE | 200 MG | TABLET | APOTEX INC | MARKETED | 02537931 |
| AURO-ESLICARBAZEPINE | 600 MG | TABLET | AURO PHARMA INC | MARKETED | 02527456 |
| AURO-ESLICARBAZEPINE | 200 MG | TABLET | AURO PHARMA INC | MARKETED | 02527421 |
| AURO-ESLICARBAZEPINE | 400 MG | TABLET | AURO PHARMA INC | MARKETED | 02527448 |
| AURO-ESLICARBAZEPINE | 800 MG | TABLET | AURO PHARMA INC | MARKETED | 02527464 |
| APTIOM | 200 MG | TABLET | SUMITOMO PHARMA CANADA, INC. | CANCELLED POST MARKET | 02426862 |
| APTIOM | 800 MG | TABLET | SUMITOMO PHARMA CANADA, INC. | CANCELLED POST MARKET | 02426897 |
2 · Same class — other molecules in ATC N03AF
| Molecule | Canadian brands | DINs | Marketed | Sourceable |
|---|---|---|---|---|
| Carbamazepine | APO-CARBAMAZEPINE · APO-CARBAMAZEPINE CR · BIO-CARBAMAZEPINE · CARBAMAZEPINE 200 TAB 200MG · +26 more | 46 | 11 | Yes |
| Oxcarbazepine | APO-OXCARBAZEPINE · JAMP OXCARBAZEPINE · JAMP-OXCARBAZEPINE · NOVO-OXCARBAZEPINE · +6 more | 22 | 9 | Yes |
| Eslicarbazepine | APO-ESLICARBAZEPINE · APTIOM · AURO-ESLICARBAZEPINE | 12 | 8 | Yes |
| Rufinamide | AURO-RUFINAMIDE · BANZEL | 6 | 5 | Yes |
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 N03A
| ATC subgroup | Molecules | DINs | Marketed |
|---|---|---|---|
| N03AX | Brivaracetam · Cannabidiol · Cenobamate · Lacosamide · Lamotrigine · +4 more | 391 | 197 |
| N03AG | Valproic Acid · Vigabatrin | 75 | 19 |
| N03AA | Phenobarbital · Primidone | 39 | 13 |
| N03AB | Fosphenytoin · Phenytoin · Phenytoin, Combinations | 17 | 8 |
| N03AE | Clonazepam | 55 | 8 |
| N03AD | Ethosuximide · Mesuximide | 5 | 4 |
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.
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.