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MIDAMOR TABLETS 5MG 5 MG — DIN 00487805

AMILORIDE HYDROCHLORIDE : 5 MG · ORBUS PHARMA INC · TABLET · wholesale supply in Canada

Health Canada status: CANCELLED POST MARKET

What is MIDAMOR TABLETS 5MG?

MIDAMOR TABLETS 5MG 5 MG contains AMILORIDE HYDROCHLORIDE : 5 MG. It is listed in the Health Canada Drug Product Database under DIN 00487805, held by ORBUS PHARMA INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 16-Jun-2010. 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.

What is MIDAMOR TABLETS 5MG used for?

Cirrhosis with ascites and edema; adjunct in edema of cardiac origin or hypertension to prevent/treat hypokalemia or maintain potassium levels.

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

How much does Amiloride cost around the world?

Amiloride is listed on 5 of the national price registers Nexara ingests. Each country publishes on a different basis, so those figures are not comparable with one another — or with a Canadian wholesale price.

What a market publishes matters more than the number it publishes. Australia publishes a ex-manufacturer; Saudi Arabia publishes a public; South Africa publishes a single exit price. Comparing an ex-factory ceiling against a pharmacy public price tells you nothing about either, and comparing either against a Canadian landed cost tells you less.

MarketPrice basis published thereBrandsPacks listedRange
South Africasingle exit price77ZAR███.██
United Statesacquisition14USD███.██
Australiaex-manufacturer12AUD███.██
United Kingdomhospital11GBP███.██
Saudi Arabiapublic11SAR███.██

15 pack listings across 11 brand entries and 5 price bases, refreshed 08 Sep 2026. Ranges span every Amiloride pack in that market, so a high figure is usually a larger pack rather than the same product.

Figures are held for the Nexara team. Cross-market prices are published on incompatible bases and are not an offer, a landed cost, or a guide to what any buyer can obtain. Nexara publishes which markets list the product and on what basis; the numbers stay internal.

Team sign-in

This table is a regulatory record of where the molecule is listed. The DIN on this page is no longer authorized for sale in Canada, so Nexara does not quote it — see the alternatives above.

Is there a generic Amiloride 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.

2 holders have a Canadian DIN containing Amiloride, across 3 DINs, of which 1 are currently marketed. Marketed count is the number that matters: an approval that is not marketed cannot be bought.

Market authorization holderDINsMarketedBrand namesPosition
AA PHARMA INC11MIDAMORSourceable in Canada
ORBUS PHARMA INC20AMILORIDE HYDROCHLORIDE TABLETS, USP, MIDAMOR TABLETS 5MGNo 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 label5 MG
Dosage formTABLET
RouteORAL
Pack configuration (monograph)Bottles of 100 tablets.
StorageNot explicitly specified in the provided text (standard practice is to refer to USP/manufacturer labels).

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 substanceAmiloride
ATC codeC03DB01
AHFS class40:20.00
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)00487805
DIN (unpadded, as printed on some documents)487805
Brand nameMIDAMOR TABLETS 5MG
Generic / active ingredientAMILORIDE HYDROCHLORIDE : 5 MG
Market authorization holderORBUS PHARMA INC
Health Canada schedulePrescription
ATC codeC03DB01
ATC anatomical main groupC — Cardiovascular system
ATC therapeutic subgroupC03DB
Current statusCANCELLED POST MARKET
Status date16-Jun-2010
Original market date1984-12-31 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?

Cirrhosis: Start 5 mg/day, max 20 mg/day. Edema/Hypertension: 5-10 mg daily with other diuretics, max 20 mg/day. Adjust based on serum potassium levels.

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

Contraindications

Hyperkalemia (serum K+ >5.5 mEq/L); use of other antikaliuretic agents or potassium salts; impaired renal function (anuria, acute renal failure, diabetic nephropathy); hypersensitivity.

Warnings and precautions

Hyperkalemia (can be fatal); monitor serum potassium carefully, especially in elderly, diabetics, or renal impairment. Discontinue 3 days before glucose tolerance tests. Risk of metabolic acidosis.

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

1 of 3 Canadian DINs for this molecule are currently marketed. Marketed products are listed first.

ProductStrengthFormHolderHealth Canada statusDIN
MIDAMOR5.0 MGTABLETAA PHARMA INCMARKETED02249510
AMILORIDE HYDROCHLORIDE TABLETS, USP5 MGTABLETORBUS PHARMA INCCANCELLED (UNRETURNED ANNUAL)02257394

2 · Same class — other molecules in ATC C03DB

MoleculeCanadian brandsDINsMarketedSourceable
AmilorideAMILORIDE HYDROCHLORIDE TABLETS, USP · MIDAMOR · MIDAMOR TABLETS 5MG31Yes
TriamtereneDYRENIUM 100 · DYRENIUM 5020Not 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.

3 · Adjacent classes in ATC C03D

ATC subgroupMoleculesDINsMarketed
C03DAEplerenone · Finerenone · Spironolactone2214

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 MIDAMOR TABLETS 5MG called?

Also recorded in Canada as: amiloride hydrochloride 5 MG Oral Tablet (US), amiloride hydrochloride 5 MG / hydrochlorothiazide 50 MG Oral Tablet (US), amiloride hydrochloride 1 MG/ML Oral Solution (US), amiloride hydrochloride 10 MG / furosemide 80 MG Oral Tablet (US), amiloride hydrochloride 2.5 MG / cyclopenthiazide 0.25 MG Oral Tablet (US), amiloride hydrochloride 2.5 MG / atenolol 50 MG / hydrochlorothiazide 25 MG Oral Capsule (US), amiloride hydrochloride 2.5 MG / furosemide 20 MG Oral Tablet (US), amiloride hydrochloride 2.5 MG / hydrochlorothiazide 25 MG / timolol maleate 10 MG Oral Tablet (US), amiloride hydrochloride 2.5 MG / hydrochlorothiazide 25 MG Oral Tablet (US), amiloride hydrochloride 5 MG / bumetanide 1 MG Oral Tablet (US), amiloride hydrochloride 5 MG / furosemide 40 MG Oral Tablet (US), AMILORIDE HYDROCHLORIDE (US), AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE (US).

The same molecule, Amiloride, is registered under other names elsewhere. Buyers and prescribers searching from outside Canada — or working from a foreign prescription or tender document — often know it by one of these:

NameScriptRegistered in
ModureticLatinAustralia, South Africa
Amiloretic H.S. TabletsLatinSouth Africa
APO-AMILZIDELatinSaudi Arabia
BetareticLatinSouth Africa
Moduretic hsLatinSouth Africa
Sandoz Co-AmilozideLatinSouth Africa
ServatrinLatinSouth Africa
Spec-Co-AmilorideLatinSouth Africa

Names are taken from national medicine registers and published price lists. A product registered abroad is not authorized for sale in Canada unless it holds its own DIN; import is possible only through the routes Health Canada permits.

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 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 00487805. Last reviewed 2026-09-10. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.