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LUTREPULSE 3.2 MG — DIN 02046202

GONADORELIN ACETATE : 3.2 MG · FERRING INC · POWDER FOR SOLUTION · wholesale supply in Canada

Health Canada status: DORMANT

What is LUTREPULSE?

LUTREPULSE 3.2 MG contains GONADORELIN ACETATE : 3.2 MG. It is listed in the Health Canada Drug Product Database under DIN 02046202, held by FERRING INC, supplied as POWDER FOR SOLUTION for INTRAVENOUS ; SUBCUTANEOUS administration. Health Canada currently lists it as dormant, status dated 21-Apr-2017. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A). This DIN is not currently being marketed in Canada, so it is sourced to order where a compliant route exists rather than held in stock.

What is LUTREPULSE used for?

LUTREPULSE (gonadorelin acetate) is indicated for the induction of ovulation in women with primary hypothalamic amenorrhea. Therapy is continued until the desired therapeutic result (follicle maturation and ovulation) is achieved. After ovulation, the therapy should be continued to support the corpus luteum function until the late luteal phase, until endogenous hCG of the implanted trophoblast maintains the function of the corpus luteum.

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

How much does Gonadorelin cost around the world?

Gonadorelin 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. Czechia publishes a max producer price (ex-factory); Iceland publishes a max wholesale. 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
Czechiamax producer price (ex-factory)11CZK███.██
Icelandmax wholesale11ISK███.██

2 pack listings across 2 brand entries and 2 price bases, refreshed 03 Sep 2026. Ranges span every Gonadorelin 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.

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Canada publishes no comparable public list price. For a delivered Canadian price on a licensed account, verify your licence — it takes about a minute.

Ask Nexara for a landed Canadian price

Is there a generic Gonadorelin 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.

Only one market authorization holder has a Canadian DIN containing Gonadorelin — 2 DINs, of which 0 are currently marketed. There is no second Canadian source today, so a supply interruption on this holder has no domestic substitute at the same molecule.

Market authorization holderDINsMarketedBrand namesPosition
FERRING INC20LUTREPULSE, LUTREPULSE PWS 0.8MG/VIALNo 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 label3.2 MG
Dosage formPOWDER FOR SOLUTION
RouteINTRAVENOUS ; SUBCUTANEOUS
Pack configuration (monograph)Three vials of 3.2 mg of gonadorelin acetate as a lyophilized, sterile powder, Three 10 mL vial of 0.9% sodium chloride injection, 3 POD devices (POD with adhesive backing, supplied with a short needle and syringe); syringe for the reconstitution with sodium chloride
Storageroom temperature (15°-30°C) in the unopened package

Before an order line is unambiguous Nexara needs the strength, the pack size and the presentation.

Substance and classification

Active substanceGonadorelin
ATC codeH01CA01
AHFS class68:18.00
Biosimilar biologicNo

Confirm the pack and get a price

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)02046202
DIN (unpadded, as printed on some documents)2046202
Brand nameLUTREPULSE
Generic / active ingredientGONADORELIN ACETATE : 3.2 MG
Market authorization holderFERRING INC
Health Canada schedulePrescription
ATC codeH01CA01
ATC anatomical main groupH — Systemic hormonal preparations
ATC therapeutic subgroupH01CA
Current statusDORMANT
Status date21-Apr-2017
Original market date1994-12-31 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

0 of 2 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
LUTREPULSE PWS 0.8MG/VIAL0.8 MGPOWDER FOR SOLUTIONFERRING INCCANCELLED POST MARKET02046210

2 · Same class — other molecules in ATC H01CA

MoleculeCanadian brandsDINsMarketedSourceable
NafarelinSYNAREL · SYNAREL NAS SOL 2MG/ML21Yes
GonadorelinLUTREPULSE · LUTREPULSE PWS 0.8MG/VIAL20Not 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 H01C

ATC subgroupMoleculesDINsMarketed
H01CBLanreotide · Octreotide · Pasireotide · Somatostatin4923
H01CCCetrorelix · Elagolix · Ganirelix · Relugolix, Estradiol And Norethisterone65

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 LUTREPULSE called?

The same molecule, Gonadorelin, 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
LHRH FerringLatinCzechia, Iceland

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.

How can I get it?

This DIN is dormant — it holds a Health Canada authorization but is not currently being marketed in Canada, so it cannot simply be ordered from Canadian stock. Where a patient need exists, supply may be possible through exceptional importation or the Special Access Programme, subject to Health Canada's requirements and the prescriber's application. Nexara can advise on the route and on marketed alternatives.

Ask about sourcing LUTREPULSE

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 02046202. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.