EPTIFIBATIDE INJECTION 2 MG — DIN 02367858
EPTIFIBATIDE : 2 MG · TEVA CANADA LIMITED · SOLUTION · wholesale supply in Canada
Health Canada status: CANCELLED POST MARKET
What is EPTIFIBATIDE INJECTION?
EPTIFIBATIDE INJECTION 2 MG contains EPTIFIBATIDE : 2 MG. It is listed in the Health Canada Drug Product Database under DIN 02367858, held by TEVA CANADA LIMITED, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as cancelled post market, status dated 30-Apr-2018. 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 Eptifibatide cost around the world?
Eptifibatide is listed on 4 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); Saudi Arabia publishes a public; South Africa publishes a single exit price. 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 Kingdom | hospital | 2 | 2 | GBP███.██ |
| South Africa | single exit price | 2 | 2 | ZAR███.██ |
| Hungary | producer price (ex-factory) | 1 | 1 | HUF███.██ |
| Saudi Arabia | public | 1 | 1 | SAR███.██ |
6 pack listings across 6 brand entries and 4 price bases, refreshed 03 Sep 2026. Ranges span every Eptifibatide 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 Eptifibatide 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.
7 holders have a Canadian DIN containing Eptifibatide, across 14 DINs, of which 2 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 |
|---|---|---|---|---|
| JUNO PHARMACEUTICALS CORP. | 2 | 2 | EPTIFIBATIDE INJECTION | Sourceable in Canada |
| ACCORD HEALTHCARE INC | 2 | 0 | EPTIFIBATIDE INJECTION | No marketed DIN |
| FRESENIUS KABI CANADA LTD | 2 | 0 | EPTIFIBATIDE INJECTION | No marketed DIN |
| MERCK CANADA INC | 2 | 0 | INTEGRILIN | No marketed DIN |
| OMEGA LABORATORIES LIMITED | 2 | 0 | EPTIFIBATIDE INJECTION | No marketed DIN |
| STRIDES PHARMA CANADA INC | 2 | 0 | EPTIFIBATIDE INJECTION | No marketed DIN |
| TEVA CANADA LIMITED | 2 | 0 | EPTIFIBATIDE INJECTION | 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 | 2 MG |
|---|---|
| Dosage form | SOLUTION |
| Route | INTRAVENOUS |
Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation.
Substance and classification
| Active substance | Eptifibatide |
|---|---|
| ATC code | B01AC16 |
| AHFS class | 20:12.18 |
| 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) | 02367858 |
|---|---|
| DIN (unpadded, as printed on some documents) | 2367858 |
| Brand name | EPTIFIBATIDE INJECTION |
| Generic / active ingredient | EPTIFIBATIDE : 2 MG |
| Market authorization holder | TEVA CANADA LIMITED |
| Health Canada schedule | Prescription |
| ATC code | B01AC16 |
| ATC anatomical main group | B — Blood and blood-forming organs |
| ATC therapeutic subgroup | B01AC |
| Current status | CANCELLED POST MARKET |
| Status date | 30-Apr-2018 |
| Original market date | 2013-04-29 00:00:00 |
| 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
2 of 14 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.
| Product | Strength | Form | Holder | Health Canada status | DIN |
|---|---|---|---|---|---|
| EPTIFIBATIDE INJECTION | 2 MG | SOLUTION | JUNO PHARMACEUTICALS CORP. | MARKETED | 02540827 |
| EPTIFIBATIDE INJECTION | 0.75 MG | Solution | JUNO PHARMACEUTICALS CORP. | MARKETED | 02540819 |
| EPTIFIBATIDE INJECTION | 0.75 MG | SOLUTION | OMEGA LABORATORIES LIMITED | CANCELLED PRE MARKET | 02410109 |
| EPTIFIBATIDE INJECTION | 2 MG | SOLUTION | OMEGA LABORATORIES LIMITED | CANCELLED PRE MARKET | 02410125 |
| EPTIFIBATIDE INJECTION | 0.75 MG | SOLUTION | STRIDES PHARMA CANADA INC | APPROVED | 02422840 |
| EPTIFIBATIDE INJECTION | 0.75 MG | SOLUTION | ACCORD HEALTHCARE INC | CANCELLED PRE MARKET | 02454483 |
| EPTIFIBATIDE INJECTION | 2 MG | SOLUTION | ACCORD HEALTHCARE INC | CANCELLED PRE MARKET | 02454491 |
| EPTIFIBATIDE INJECTION | 0.75 MG | SOLUTION | FRESENIUS KABI CANADA LTD | CANCELLED PRE MARKET | 02460378 |
| EPTIFIBATIDE INJECTION | 2 MG | SOLUTION | FRESENIUS KABI CANADA LTD | CANCELLED PRE MARKET | 02460386 |
| EPTIFIBATIDE INJECTION | 2 MG | SOLUTION | STRIDES PHARMA CANADA INC | APPROVED | 02422859 |
2 · Same class — other molecules in ATC B01AC
| Molecule | Canadian brands | DINs | Marketed | Sourceable |
|---|---|---|---|---|
| Clopidogrel | ABBOTT-CLOPIDOGREL · ACCEL-CLOPIDOGREL · ACT CLOPIDOGREL · AG-CLOPIDOGREL · APO-CLOPIDOGREL · AURO-CLOPIDOGREL · BIO-CLOPIDOGREL · CLOPIDOGREL · DOM-CLOPIDOGREL · IPG-CLOPIDOGREL · JAMP-CLOPIDOGREL · M-CLOPIDOGREL · MAR-CLOPIDOGREL · MINT-CLOPIDOGREL · MYLAN-CLOPIDOGREL · NRA-CLOPIDOGREL · PLAVIX · PMS-CLOPIDOGREL · PRIVA-CLOPIDOGREL · Q-CLOPIDOGREL · RBX-CLOPIDOGREL · RIVA-CLOPIDOGREL · SANDOZ CLOPIDOGREL · TARO-CLOPIDOGREL · TEVA-CLOPIDOGREL · TORRENT-CLOPIDOGREL | 39 | 19 | Yes |
| Acetylsalicylic Acid | APO-ASA LD · ASA · ASA 81 MG · ASA DAILY LOW DOSE · ASA EC · ASAPHEN EC · ASPIRIN 81MG · ASPIRIN 81MG QUICK CHEWS · CHEWABLE DAILY LOW DOSE ASA · COATED DAILY LOW DOSE ASA 81 MG · ENTERIC COATED ASA DAILY LOW DOSE · ENTERIC COATED DAILY LOW DOSE ASA 81 MG · ENTROPHEN · ENTROPHEN CHEWABLE · EQUATE DAILY LOW-DOSE · EXACT COATED DAILY LOW-DOSE ASA · JAMP-ASA 81MG EC · LONDON DRUGS COATED DAILY LOW-DOSE ASA · PMS-ASA · PRAXIS ASA EC 81 MG DAILY LOW DOSE · RIVASA 81 MG EC | 23 | 12 | Yes |
| Ticagrelor | AG-TICAGRELOR · APO-TICAGRELOR · BRILINTA · JAMP TICAGRELOR · M-TICAGRELOR · TARO-TICAGRELOR · TEVA-TICAGRELOR | 14 | 12 | Yes |
| Selexipag | UPTRAVI | 8 | 8 | Yes |
| Treprostinil | REMODULIN · TREPROSTINIL INJECTION | 8 | 4 | Yes |
| Epoprostenol | CARIPUL · EPOPROSTENOL FOR INJECTION · FLOLAN | 6 | 4 | Yes |
| Dipyridamole | APO-DIPYRIDAMOLE · APO-DIPYRIDAMOLE-SC TAB 25MG · APO-DIPYRIDAMOLE-SC TAB 50MG · APO-DIPYRIDAMOLE-SC TAB 75MG · DIPYRIDAMOLE 25 TAB 25MG · DIPYRIDAMOLE 50 TAB 50MG · DIPYRIDAMOLE 75 TAB · DIPYRIDAMOLE FOR INJECTION · DIPYRIDAMOLE INJECTION, USP · DIPYRIDAMOLE-25 · DIPYRIDAMOLE-50 · DIPYRIDAMOLE-75 · NOVO-DIPIRADOL SCT 100MG · NOVO-DIPIRADOL TAB 25MG · NOVO-DIPIRADOL TAB 50MG · NOVO-DIPIRADOL TAB 75MG · PERSANTINE · PERSANTINE TAB 100MG · PERSANTINE TAB 25MG · PERSANTINE TAB 50MG · PERSANTINE TAB 75MG | 24 | 2 | Yes |
| Eptifibatide | EPTIFIBATIDE INJECTION · INTEGRILIN | 14 | 2 | Yes |
| Tirofiban | AGGRASTAT | 2 | 1 | Yes |
| Prasugrel | EFFIENT · JAMP PRASUGREL | 2 | 1 | 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 B01A
| ATC subgroup | Molecules | DINs | Marketed |
|---|---|---|---|
| B01AF | Apixaban · Edoxaban · Rivaroxaban | 159 | 121 |
| B01AB | Antithrombin · Dalteparin · Danaparoid · Enoxaparin · Heparin · Heparin, Combinations · Nadroparin · Tinzaparin | 128 | 82 |
| B01AA | Acenocoumarol · Warfarin | 62 | 16 |
| B01AE | Argatroban · Bivalirudin · Dabigatran Etexilate · Lepirudin | 18 | 11 |
| B01AX | Caplacizumab · Defibrotide · Fondaparinux | 10 | 5 |
| B01AD | Alteplase · Ancrod · Anistreplase · Drotrecogin Alfa · Reteplase · Streptokinase · Tenecteplase · Urokinase | 22 | 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.
What else is EPTIFIBATIDE INJECTION called?
The same molecule, Eptifibatide, 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 |
|---|---|---|
| Eptifibatide Hainan | Latin | Saudi Arabia |
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.