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REHYDRALYTE 25 MG — DIN 00763195

DEXTROSE : 25 MG POTASSIUM CITRATE : 2.04 MG SODIUM CHLORIDE : 3.8 MG SODIUM CITRATE : .78 MG · ROSS LABORATORIES, DIVISION OF ABBOTT LABORATORIES LTD. · LIQUID · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is REHYDRALYTE?

REHYDRALYTE 25 MG contains DEXTROSE : 25 MG POTASSIUM CITRATE : 2.04 MG SODIUM CHLORIDE : 3.8 MG SODIUM CITRATE : .78 MG. It is listed in the Health Canada Drug Product Database under DIN 00763195, held by ROSS LABORATORIES, DIVISION OF ABBOTT LABORATORIES LTD., supplied as LIQUID for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 16-Apr-2008. This Drug Identification Number is no longer authorized for sale in Canada, so Nexara does not supply it. The record is kept here because buyers still meet the number on old formularies, purchase orders and tender documents; Nexara can help identify an authorized alternative.

Is there a generic Oral Rehydration Salt Formulations 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.

4 holders have a Canadian DIN containing Oral Rehydration Salt Formulations, across 5 DINs, of which 0 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
MEAD JOHNSON NUTRITIONALS20LYTREN, LYTREN RHS LIQNo marketed DIN
AVENTIS PHARMA INC10GASTROLYTENo marketed DIN
IAMAT (INTER ASSOC MEDIC ASSIST TRAVEL)10DIALYTENo marketed DIN
ROSS LABORATORIES, DIVISION OF ABBOTT LABORATORIES LTD.10REHYDRALYTENo 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 label25 MG
Dosage formLIQUID
RouteORAL

Pack detail is kept as a regulatory record. This DIN is no longer authorized for sale in Canada, so Nexara does not quote this pack.

Substance and classification

Active substanceOral Rehydration Salt Formulations
ATC codeA07CA
AHFS class40:12.00
Biosimilar biologicNo

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)00763195
DIN (unpadded, as printed on some documents)763195
Brand nameREHYDRALYTE
Generic / active ingredientDEXTROSE : 25 MG POTASSIUM CITRATE : 2.04 MG SODIUM CHLORIDE : 3.8 MG SODIUM CITRATE : .78 MG
Market authorization holderROSS LABORATORIES, DIVISION OF ABBOTT LABORATORIES LTD.
Health Canada scheduleNON-PRESCRIPTION DRUGS
ATC codeA07CA
ATC anatomical main groupA — Alimentary tract and metabolism
ATC therapeutic subgroupA07CA
Current statusCANCELLED POST MARKET
Status date16-Apr-2008
Original market date1988-12-31 00:00:00
Status sourceLive Health Canada DPD sync

Verify on the primary sources

Health Canada DPD record

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

ProductStrengthFormHolderHealth Canada statusDIN
DIALYTE3.5 GPOWDER FOR SOLUTIONIAMAT (INTER ASSOC MEDIC ASSIST TRAVEL)CANCELLED POST MARKET00574880
GASTROLYTE470 MGPOWDER FOR SOLUTIONAVENTIS PHARMA INCCANCELLED POST MARKET01931555
LYTREN2 G / 100 MLLIQUIDMEAD JOHNSON NUTRITIONALSCANCELLED POST MARKET00654957
LYTREN RHS LIQ375 MG / 100 MLLIQUIDMEAD JOHNSON NUTRITIONALSCANCELLED POST MARKET00841803

2 · Same class — other molecules in ATC A07CA

MoleculeCanadian brandsDINsMarketedSourceable
Oral Rehydration Salt FormulationsDIALYTE · GASTROLYTE · LYTREN · LYTREN RHS LIQ · +1 more50Not 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.

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 REHYDRALYTE called?

Also recorded in Canada as: glucose 0.4 MG/MG Oral Gel [Glutose] (US), glucose 50 MG/ML Oral Solution [Enfamil Glucose] (US), glucose 4000 MG Chewable Tablet [Dex4] (US), glucose 0.4 MG/MG Oral Gel [Glucoburst] (US), cholecalciferol 6.67 UNT/ML / glucose 250 MG/ML Oral Solution [ReliOn Glucose] (US), glucose 1000 MG Chewable Tablet [Dex4] (US), glucose 0.774 MG/MG Oral Gel [Insta-Glucose] (US), glucose 0.45 MG/MG Oral Gel [Dex4] (US), glucose 254 MG/ML Oral Solution [Dex4] (US), glucose 0.4 MG/MG Oral Gel [Dex4] (US), fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution [Emetrol] (US), fructose 175 MG / glucose 968 MG / sodium citrate 230 MG Chewable Tablet (US), glucose 166.7 MG/ML Oral Solution (US), glucose 150 MG/ML Injectable Solution (US), cholecalciferol 6.67 UNT/ML / glucose 250 MG/ML Oral Solution (US).

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. 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. 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 00763195. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.