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FUNGIZONE 50 MG — DIN 00029149

AMPHOTERICIN B : 50 MG · CHEPLAPHARM ARZNEIMITTEL GMBH · POWDER FOR SOLUTION · wholesale supply in Canada

Health Canada status: MARKETED

What is FUNGIZONE?

FUNGIZONE 50 MG contains AMPHOTERICIN B : 50 MG. It is listed in the Health Canada Drug Product Database under DIN 00029149, held by CHEPLAPHARM ARZNEIMITTEL GMBH, supplied as POWDER FOR SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 02-Jan-2020. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.

What is FUNGIZONE used for?

FUNGIZONE (amphotericin B) is specifically intended for the treatment of disseminated mycotic infections, including coccidioidomycosis; cryptococcosis (torulosis); disseminated candidiasis, histoplasmosis, South American leishmaniasis, North and South American blastomycosis; mucormycosis (phycomycosis) caused by species of the genera Mucor, Rhizopus, Absidia, Entomophthora, and Basidiobolus, sporotrichosis (Sporotrichum schenckii), and aspergillosis (Aspergillus fumigatus). Limited studies have shown that amphotericin B powder for injection may be useful when administered by routes other than intravenous for the treatment of certain types of fungal infections.

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

Is there a generic Amphotericin B 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.

6 holders have a Canadian DIN containing Amphotericin B, across 7 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 holderDINsMarketedBrand namesPosition
ASTELLAS PHARMA CANADA INC11AMBISOMESourceable in Canada
CHEPLAPHARM ARZNEIMITTEL GMBH11FUNGIZONESourceable in Canada
THREE RIVERS PHARMACEUTICALS LLC20AMPHOTEC 100 MG, AMPHOTEC 50 MGNo marketed DIN
LEADIANT BIOSCIENCES, INC10ABELCETNo marketed DIN
STERIMAX INC10AMPHOTERICIN B FOR INJECTION, USPNo marketed DIN
TARO PHARMACEUTICALS INC10TARO-AMPHOTERICIN B LIPOSOMALNo 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 label50 MG
Dosage formPOWDER FOR SOLUTION
RouteINTRAVENOUS
Pack configuration (monograph)null
Storagenull

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

Substance and classification

Active substanceAmphotericin B
ATC codeJ02AA01
AHFS class28:16.08.24
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)00029149
DIN (unpadded, as printed on some documents)29149
Brand nameFUNGIZONE
Generic / active ingredientAMPHOTERICIN B : 50 MG
Market authorization holderCHEPLAPHARM ARZNEIMITTEL GMBH
Health Canada schedulePrescription
ATC codeJ02AA01
ATC anatomical main groupJ — Anti-infectives for systemic use
ATC therapeutic subgroupJ02AA
Current statusMARKETED
Status date02-Jan-2020
Original market date1968-12-31 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record Approved product monograph (PDF)

How is it administered?

Slow IV infusion over 2-6 hours. Recommended concentration 0.1 mg/mL in 5% Dextrose. Dosage must be individualized; do not exceed 1.5 mg/kg/day. Test dose (1 mg) often preferred.

Included because it drives pack selection and wastage. Consult the monograph.

Contraindications

Hypersensitivity to amphotericin B or any component unless the condition is life-threatening and amenable only to this therapy.

Warnings and precautions

Specifically for progressive, potentially fatal infections. Exercise caution to prevent inadvertent overdose (fatal cardiac arrest). Avoid rapid infusion (<1 hour). Monitor renal function.

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

ProductStrengthFormHolderHealth Canada statusDIN
AMBISOME50 MGPOWDER FOR SOLUTIONASTELLAS PHARMA CANADA INCMARKETED02241630
ABELCET5 MGSUSPENSIONLEADIANT BIOSCIENCES, INCCANCELLED POST MARKET02231590
AMPHOTEC 100 MG100 MGPOWDER FOR SUSPENSIONTHREE RIVERS PHARMACEUTICALS LLCCANCELLED POST MARKET02241749
AMPHOTEC 50 MG50 MGPOWDER FOR SUSPENSIONTHREE RIVERS PHARMACEUTICALS LLCCANCELLED POST MARKET02241750
AMPHOTERICIN B FOR INJECTION, USP50 MGPOWDER FOR SOLUTIONSTERIMAX INCAPPROVED02405032
TARO-AMPHOTERICIN B LIPOSOMAL50 MGPOWDER FOR SOLUTIONTARO PHARMACEUTICALS INCAPPROVED02554186

2 · Same class — other molecules in ATC J02AA

MoleculeCanadian brandsDINsMarketedSourceable
Amphotericin BABELCET &middot; AMBISOME &middot; AMPHOTEC 100 MG &middot; AMPHOTEC 50 MG &middot; +3 more72Yes

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 J02A

ATC subgroupMoleculesDINsMarketed
J02ACFluconazole &middot; Isavuconazole &middot; Itraconazole &middot; Posaconazole &middot; Voriconazole11554
J02AXAnidulafungin &middot; Caspofungin &middot; Micafungin2512
J02ABKetoconazole52

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.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

Request a quote for FUNGIZONE

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 00029149. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.