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PROCAINAMIDE-250 CAP 250MG 250 MG

PROCAINAMIDE HYDROCHLORIDE : 250 MG · DIN 00731382 · PRO DOC LIMITEE

Health Canada status: CANCELLED POST MARKET

What is PROCAINAMIDE-250 CAP 250MG?

PROCAINAMIDE-250 CAP 250MG 250 MG contains PROCAINAMIDE HYDROCHLORIDE : 250 MG. It is listed in the Health Canada Drug Product Database under DIN 00731382, held by PRO DOC LIMITEE, supplied as CAPSULE for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 31-Jul-2000. 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

DIN00731382
Brand namePROCAINAMIDE-250 CAP 250MG
Generic / active ingredientPROCAINAMIDE HYDROCHLORIDE : 250 MG
ManufacturerPRO DOC LIMITEE
Strength250 MG
Dosage formCAPSULE
Route of administrationORAL
SchedulePrescription
ATC codeC01BA02 PROCAINAMIDE
AHFS class24:04.04.04
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date31-Jul-2000
Original market date1987-12-31 00:00:00

What can be used instead?

Other Canadian products sharing ATC code C01BA02 PROCAINAMIDE. 1 of 15 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
PROCAINAMIDE HYDROCHLORIDE INJECTION USP100 MGSOLUTIONSANDOZ CANADA INCORPORATEDMARKETEDDIN 02184486
APO-PROCAINAMIDE CAP 250MG250 MGCAPSULEAPOTEX INCCANCELLED POST MARKETDIN 00713325
APO-PROCAINAMIDE CAP 375MG375 GCAPSULEAPOTEX INCCANCELLED POST MARKETDIN 00713333
APO-PROCAINAMIDE CAP 500MG500 MGCAPSULEAPOTEX INCCANCELLED POST MARKETDIN 00713341
PROCAINAMIDE-375 CAP 375MG375 MGCAPSULEPRO DOC LIMITEECANCELLED POST MARKETDIN 00731390
PROCAINAMIDE-500 CAP 500MG500 MGCAPSULEPRO DOC LIMITEECANCELLED POST MARKETDIN 00728268
PROCAN SR250 MGTABLET (EXTENDED-RELEASE)SEARCHLIGHT PHARMA INCCANCELLED POST MARKETDIN 00638692
PROCAN SR500 MGTABLET (EXTENDED-RELEASE)ERFA CANADA 2012 INCCANCELLED POST MARKETDIN 00638676
PROCAN SR750 MGTABLET (EXTENDED-RELEASE)ERFA CANADA 2012 INCCANCELLED POST MARKETDIN 00638684
PRONESTYL CAP 250MG250 MGCAPSULESQUIBB CANADA INC., DIVISION OF BRISTOL-MYERS SQUIBB CANADA INC.CANCELLED POST MARKETDIN 00029076

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 00731382. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.