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DT POLIO ADSORBED - SUS IM 25 LF / 0.5 ML

DIPHTHERIA TOXOID : 25 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 1 MAHONEY : 40 UNIT / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 3 SAUKETT : 32 UNIT / 0.5 ML TETANUS TOXOID : 5 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 2 MEF1 : 8 UNIT / 0.5 ML · DIN 02189127 · AVENTIS PASTEUR LIMITED

Health Canada status: CANCELLED POST MARKET

What is DT POLIO ADSORBED - SUS IM?

DT POLIO ADSORBED - SUS IM 25 LF / 0.5 ML contains DIPHTHERIA TOXOID : 25 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 1 MAHONEY : 40 UNIT / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 3 SAUKETT : 32 UNIT / 0.5 ML TETANUS TOXOID : 5 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 2 MEF1 : 8 UNIT / 0.5 ML. It is listed in the Health Canada Drug Product Database under DIN 02189127, held by AVENTIS PASTEUR LIMITED, supplied as SUSPENSION for INTRAMUSCULAR administration. Health Canada currently lists it as cancelled post market, status dated 17-Jul-2006. 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

DIN02189127
Brand nameDT POLIO ADSORBED - SUS IM
Generic / active ingredientDIPHTHERIA TOXOID : 25 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 1 MAHONEY : 40 UNIT / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 3 SAUKETT : 32 UNIT / 0.5 ML TETANUS TOXOID : 5 LF / 0.5 ML INACTIVATED POLIOMYELITIS VACCINE (D.C.O.) TYPE 2 MEF1 : 8 UNIT / 0.5 ML
ManufacturerAVENTIS PASTEUR LIMITED
Strength25 LF / 0.5 ML
Dosage formSUSPENSION
Route of administrationINTRAMUSCULAR
ScheduleSchedule D
ATC codeJ07CA01 DIPHTHERIA-POLIOMYELITIS-TETANUS
AHFS class80:12.00
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date17-Jul-2006
Original market date1996-12-12 00:00:00

What can be used instead?

Other Canadian products sharing ATC code J07CA01 DIPHTHERIA-POLIOMYELITIS-TETANUS. 0 of 2 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
TD POLIO ADSORBED40 UNIT / 0.5 MLSUSPENSIONSANOFI PASTEUR LIMITEDCANCELLED POST MARKETDIN 00615358

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 02189127. Last reviewed 2026-09-09. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.