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SANDOZ GEFITINIB 250 MG — DIN 02487748

GEFITINIB : 250 MG · SANDOZ CANADA INCORPORATED · TABLET · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is SANDOZ GEFITINIB?

SANDOZ GEFITINIB 250 MG contains GEFITINIB : 250 MG. It is listed in the Health Canada Drug Product Database under DIN 02487748, held by SANDOZ CANADA INCORPORATED, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 31-Jul-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 SANDOZ GEFITINIB used for?

Sandoz Gefitinib (gefitinib) is indicated for the first line treatment of patients with locally advanced (not amenable to curative therapy) or metastatic non-small cell lung cancer (NSCLC) who have activating mutations of the EGFR-TK.

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

How much does Gefitinib cost around the world?

Gefitinib 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; Bahrain publishes a retail (max); Brazil publishes a preco fabrica (ex-factory ceiling). 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.

MarketPrice basis published thereBrandsPacks listedRange
Hungaryproducer price (ex-factory)44HUF███.██
SwedenAIP (pharmacy purchase price)34SEK███.██
Italyex-factory (classe H)23EUR███.██
Romaniamax producer price33RON███.██
Australiaex-manufacturer12AUD███.██
Greeceproducer price (ex-factory)22EUR███.██
Saudi Arabiapublic22SAR███.██
Bahrainretail (max)11BHD███.██
Brazilpreco fabrica (ex-factory ceiling)11BRL███.██
United Kingdomhospital11GBP███.██
Slovakiacategorised final price11EUR███.██
South Africasingle exit price11ZAR███.██

25 pack listings across 22 brand entries and 11 price bases, refreshed 08 Sep 2026. Ranges span every Gefitinib pack in that market, so a high figure is usually a larger pack rather than the same product.

Figures are held for the Nexara team. Cross-market prices are published on incompatible bases and are not an offer, a landed cost, or a guide to what any buyer can obtain. Nexara publishes which markets list the product and on what basis; the numbers stay internal.

Team sign-in

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 Gefitinib 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 Gefitinib, across 7 DINs, of which 3 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
APOTEX INC11APO-GEFITINIBSourceable in Canada
ASTRAZENECA CANADA INC11IRESSASourceable in Canada
JAMP PHARMA CORPORATION11JAMP GEFITINIBSourceable in Canada
AURO PHARMA INC10AURO-GEFITINIBNo marketed DIN
EUGIA PHARMA INC.10EUGIA-GEFITINIBNo marketed DIN
NATCO PHARMA (CANADA) INC10NAT-GEFITINIBNo marketed DIN
SANDOZ CANADA INCORPORATED10SANDOZ GEFITINIBNo 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 label250 MG
Dosage formTABLET
RouteORAL
Pack configuration (monograph)blister packs of 30 tablets
Storagenull

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 substanceGefitinib
ATC codeL01EB01
AHFS class10:00.00
Biosimilar biologicNo

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)02487748
DIN (unpadded, as printed on some documents)2487748
Brand nameSANDOZ GEFITINIB
Generic / active ingredientGEFITINIB : 250 MG
Market authorization holderSANDOZ CANADA INCORPORATED
Health Canada schedulePrescription
ATC codeL01EB01
ATC anatomical main groupL — Antineoplastic and immunomodulating agents
ATC therapeutic subgroupL01EB
Current statusCANCELLED POST MARKET
Status date31-Jul-2026
Original market date2019-06-26 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

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

3 of 7 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
APO-GEFITINIB250 MGTABLETAPOTEX INCMARKETED02468050
IRESSA250 MGTABLETASTRAZENECA CANADA INCMARKETED02248676
JAMP GEFITINIB250 MGTABLETJAMP PHARMA CORPORATIONMARKETED02500663
AURO-GEFITINIB250 MGTABLETAURO PHARMA INCAPPROVED02533685
EUGIA-GEFITINIB250 MGTABLETEUGIA PHARMA INC.APPROVED02547546
NAT-GEFITINIB250 MGTABLETNATCO PHARMA (CANADA) INCDORMANT02491796

2 · Same class — other molecules in ATC L01EB

MoleculeCanadian brandsDINsMarketedSourceable
AfatinibGIOTRIF · MAR-AFATINIB · SANDOZ AFATINIB · TEVA-AFATINIB129Yes
ErlotinibAPO-ERLOTINIB · NAT-ERLOTINIB · PMS-ERLOTINIB · TARCEVA · +1 more147Yes
GefitinibAPO-GEFITINIB · AURO-GEFITINIB · EUGIA-GEFITINIB · IRESSA · +3 more73Yes
LazertinibLAZCLUZE22Yes
OsimertinibTAGRISSO22Yes
DacomitinibVIZIMPRO30Not 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 L01E

ATC subgroupMoleculesDINsMarketed
L01EXAvapritinib · Cabozantinib · Capivasertib · Capmatinib · Entrectinib · +17 more8064
L01EAAsciminib · Bosutinib · Dasatinib · Imatinib · Nilotinib · +1 more7357
L01EFAbemaciclib · Palbociclib · Ribociclib1714
L01EDAlectinib · Brigatinib · Ceritinib · Crizotinib · Lorlatinib1010
L01EJFedratinib · Momelotinib · Ruxolitinib88
L01EEBinimetinib · Cobimetinib · Selumetinib · Trametinib87
L01ENErdafitinib · Infigratinib · Pemigatinib116
L01ECDabrafenib · Encorafenib · Vemurafenib55

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 SANDOZ GEFITINIB called?

The same molecule, Gefitinib, 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:

NameScriptRegistered in
Cipla GefitinibLatinAustralia
IRESSALatinSweden
GEFIBLatinBrazil
GefirixLatinSouth Africa
Gefitinib AccordLatinSweden
Gefitinib STADALatinSweden
LunginibLatinSaudi Arabia
REFETIBLatinBahrain

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.

Sources and disclaimer

Product data sourced from the Health Canada Drug Product Database and the approved product monograph (PDF). Health Canada status reconciled against the live DPD sync. Last reviewed 10 Sep 2026.

Nothing on this page is medical advice. Nexara Health is a licensed wholesale distributor and supplies licensed entities only; consumer orders are routed to a partner pharmacy. Alternatives tables describe supply, not clinical equivalence.

Health Canada Drug Product Database (DPD), DIN 02487748. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.