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PODOFILM LIQ 250MG/ML 250 MG

PODOPHYLLIN : 250 MG · DIN 00598208 · PALADIN PHARMA INC.

Health Canada status: CANCELLED POST MARKET

What is PODOFILM LIQ 250MG/ML?

PODOFILM LIQ 250MG/ML 250 MG contains PODOPHYLLIN : 250 MG. It is listed in the Health Canada Drug Product Database under DIN 00598208, held by PALADIN PHARMA INC., supplied as LIQUID for TOPICAL administration. Health Canada currently lists it as cancelled post market, status dated 28-Jul-2021. 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.

Product details and regulatory record

DIN00598208
Brand namePODOFILM LIQ 250MG/ML
Generic / active ingredientPODOPHYLLIN : 250 MG
ManufacturerPALADIN PHARMA INC.
Strength250 MG
Dosage formLIQUID
Route of administrationTOPICAL
SchedulePrescription
ATC codeD06BB04 PODOPHYLLOTOXIN
AHFS class84:92.00
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date28-Jul-2021
Original market date1984-12-31 00:00:00

What can be used instead?

Other Canadian products sharing ATC code D06BB04 PODOPHYLLOTOXIN. 0 of 3 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.

ProductStrengthFormManufacturerHealth Canada statusDIN
CONDYLINE0.5 %SOLUTIONSANOFI-AVENTIS CANADA INCCANCELLED POST MARKETDIN 01945149
WARTEC5 MGLIQUIDSTIEFEL LABORATORIES (IRELAND) LIMITEDCANCELLED POST MARKETDIN 02074788

Who else supplies PODOPHYLLOTOXIN worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. PODOPHYLLOTOXIN appears in 663 registered pack listings across 3 markets, published on 3 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.

Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.

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.

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.

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.

Health Canada Drug Product Database (DPD), DIN 00598208. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.