REVOLADE 12.5 MG — DIN 02461382
ELTROMBOPAG (ELTROMBOPAG OLAMINE) : 12.5 MG · NOVARTIS PHARMACEUTICALS CANADA INC · TABLET · wholesale supply in Canada
Health Canada status: CANCELLED PRE MARKET
What is REVOLADE?
REVOLADE 12.5 MG contains ELTROMBOPAG (ELTROMBOPAG OLAMINE) : 12.5 MG. It is listed in the Health Canada Drug Product Database under DIN 02461382, held by NOVARTIS PHARMACEUTICALS CANADA INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled pre market, status dated 11-Mar-2020. 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.
How much does Eltrombopag cost around the world?
Eltrombopag 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); Czechia publishes a max producer price (ex-factory). 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 |
|---|---|---|---|---|
| Austria | KVP (Kassenverkaufspreis) | 21 | 42 | EUR███.██ |
| Greece | producer price (ex-factory) | 39 | 39 | EUR███.██ |
| Sweden | AIP (pharmacy purchase price) | 10 | 29 | SEK███.██ |
| Slovakia | categorised final price | 22 | 22 | EUR███.██ |
| Italy | ex-factory (classe H) | 9 | 21 | EUR███.██ |
| Czechia | max producer price (ex-factory) | 9 | 19 | CZK███.██ |
| Australia | ex-manufacturer | 1 | 16 | AUD███.██ |
| Hungary | producer price (ex-factory) | 16 | 16 | HUF███.██ |
| Romania | max producer price | 8 | 8 | RON███.██ |
| Morocco | PPV (public price) | 2 | 4 | MAD███.██ |
| United Kingdom | hospital | 3 | 3 | GBP███.██ |
| Luxembourg | reimbursement | 2 | 2 | EUR███.██ |
221 pack listings across 142 brand entries and 11 price bases, refreshed 08 Sep 2026. Ranges span every Eltrombopag 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 Eltrombopag 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 Eltrombopag, across 8 DINs, of which 4 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 |
|---|---|---|---|---|
| NOVARTIS PHARMACEUTICALS CANADA INC | 4 | 2 | REVOLADE | Sourceable in Canada |
| APOTEX INC | 2 | 2 | APO-ELTROMBOPAG | Sourceable in Canada |
| TEVA CANADA LIMITED | 2 | 0 | TEVA-ELTROMBOPAG | 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 | 12.5 MG |
|---|---|
| Dosage form | TABLET |
| Route | ORAL |
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 | Eltrombopag |
|---|---|
| ATC code | B02BX05 |
| 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) | 02461382 |
|---|---|
| DIN (unpadded, as printed on some documents) | 2461382 |
| Brand name | REVOLADE |
| Generic / active ingredient | ELTROMBOPAG (ELTROMBOPAG OLAMINE) : 12.5 MG |
| Market authorization holder | NOVARTIS PHARMACEUTICALS CANADA INC |
| Health Canada schedule | Prescription |
| ATC code | B02BX05 |
| ATC anatomical main group | B — Blood and blood-forming organs |
| ATC therapeutic subgroup | B02BX |
| Current status | CANCELLED PRE MARKET |
| Status date | 11-Mar-2020 |
| Status source | Live Health Canada DPD sync |
Verify on the primary sources
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
4 of 8 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.
| Product | Strength | Form | Holder | Health Canada status | DIN |
|---|---|---|---|---|---|
| APO-ELTROMBOPAG | 25 MG | TABLET | APOTEX INC | MARKETED | 02506742 |
| APO-ELTROMBOPAG | 50 MG | TABLET | APOTEX INC | MARKETED | 02506769 |
| REVOLADE | 25 MG | TABLET | NOVARTIS PHARMACEUTICALS CANADA INC | MARKETED | 02361825 |
| REVOLADE | 50 MG | TABLET | NOVARTIS PHARMACEUTICALS CANADA INC | MARKETED | 02361833 |
| REVOLADE | 75 MG | TABLET | NOVARTIS PHARMACEUTICALS CANADA INC | CANCELLED PRE MARKET | 02423049 |
| TEVA-ELTROMBOPAG | 50 MG | TABLET | TEVA CANADA LIMITED | APPROVED | 02551748 |
| TEVA-ELTROMBOPAG | 25 MG | TABLET | TEVA CANADA LIMITED | APPROVED | 02551721 |
2 · Same class — other molecules in ATC B02BX
| Molecule | Canadian brands | DINs | Marketed | Sourceable |
|---|---|---|---|---|
| Emicizumab | HEMLIBRA | 6 | 6 | Yes |
| Eltrombopag | APO-ELTROMBOPAG · REVOLADE · TEVA-ELTROMBOPAG | 8 | 4 | Yes |
| Fostamatinib | TAVALISSE | 2 | 2 | Yes |
| Romiplostim | NPLATE | 2 | 2 | Yes |
| Avatrombopag | DOPTELET | 1 | 1 | Yes |
| Concizumab | ALHEMO | 4 | 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 B02B
| ATC subgroup | Molecules | DINs | Marketed |
|---|---|---|---|
| B02BD | Catridecacog · Coagulation Factor Ix · Coagulation Factor Ix, Ii, Vii And X In Comb · Coagulation Factor Viia · Coagulation Factor Viii · +8 more | 216 | 73 |
| B02BC | Combinations · Epinephrine · Local Hemostatics · Thrombin | 23 | 6 |
| B02BA | Phytomenadione | 5 | 2 |
| B02BB | Fibrinogen, Human | 2 | 2 |
4 · Fixed-dose combinations with Canadian supply
| Product | Active ingredients | Holder | Status | DIN |
|---|---|---|---|---|
| ADYNOVATE | ANTIHEMOPHILIC FACTOR (RECOMBINANT), PEGYLATED : 1000 UNIT | TAKEDA CANADA INC | MARKETED | 02498588 |
| ALPROLIX | RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN : 500 UNIT | SANOFI-AVENTIS CANADA INC | MARKETED | 02422913 |
| ALTUVIIIO | *ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, BDD), FC-VWF-XTEN FUSION PROTEIN : 4000 UNIT | SANOFI-AVENTIS CANADA INC | MARKETED | 02448157 |
| ELOCTATE | ANTIHEMOPHILIC FACTOR (RECOMBINANT BDD), FC FUSION PROTEIN : 500 UNIT | SANOFI-AVENTIS CANADA INC | MARKETED | 02430304 |
| ESPEROCT | ANTIHEMOPHILIC FACTOR VIII (RECOMBINANT, B-DOMAIN TRUNCATED), PEGYLATED : 2000 UNIT | NOVO NORDISK CANADA INC | MARKETED | 02490099 |
| JIVI | ANTIHEMOPHILIC FACTOR (RECOMBINANT, B-DOMAIN DELETED, PEGYLATED) : 1000 UNIT | BAYER INC | MARKETED | 02481774 |
| REBINYN | COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED : 3000 UNIT | NOVO NORDISK CANADA INC | MARKETED | 02532964 |
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 REVOLADE called?
The same molecule, Eltrombopag, 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 |
|---|---|---|
| Eltrombopag Accord | Latin | Czechia, Sweden |
| Eltrombopag Viatris | Latin | Czechia, Sweden |
| Eltrombopag Avansor | Latin | Sweden |
| Eltrombopag Teva | Latin | Czechia, Sweden |
| Eltrombopag Glenmark | Latin | Sweden |
| Eltrombopag Krka | Latin | Sweden |
| Eltrombopag STADA | Latin | Sweden |
| Eltrombopag Zentiva | Latin | Sweden |
| Eltrombopag Bioglan | Latin | Sweden |
| ELTROMBOPAG OLAINFARM | Latin | Czechia |
| ELTROMBOPAG OLPHA | Latin | Czechia |
| ELTROMBOPAG VIPHARM | Latin | Czechia |
| MINING | Latin | Czechia |
| TOCIETA | Latin | Czechia |
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 pre 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.