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ALDACTONE 25 MG 25 MG

SPIRONOLACTONE : 25 MG · DIN 00028606 · PFIZER CANADA ULC

Health Canada status: CANCELLED POST MARKET

What is ALDACTONE 25 MG?

ALDACTONE 25 MG 25 MG contains SPIRONOLACTONE : 25 MG. It is listed in the Health Canada Drug Product Database under DIN 00028606, held by PFIZER CANADA ULC, supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 17-Jul-2026. 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.

What is ALDACTONE 25 MG used for?

ALDACTONE (spironolactone) is indicated for the diagnosis of primary hyperaldosteronism, management of edema and sodium retention in Congestive Heart Failure (CHF), treatment of cirrhosis of the liver accompanied by edema and/or ascites, inducing diuresis in patients with nephrotic syndrome unresponsive to other therapies, essential hypertension (usually in combination with other drugs), and treatment/prophylaxis of hypokalemia when other measures are inappropriate or inadequate.

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

Product details and regulatory record

DIN00028606
Brand nameALDACTONE 25 MG
Generic / active ingredientSPIRONOLACTONE : 25 MG
ManufacturerPFIZER CANADA ULC
Strength25 MG
Dosage formTABLET
Route of administrationORAL
SchedulePrescription
ATC codeC03DA01 SPIRONOLACTONE
AHFS class24:32.20
BiosimilarNo
Health Canada statusCANCELLED POST MARKET
Status date17-Jul-2026
Original market date1959-12-31 00:00:00

How is it administered?

Adults: 25-400 mg daily depending on indication. Primary hyperaldosteronism: 100-400 mg. Edema: 100 mg (range 25-200 mg). Hypertension: 50-100 mg. Hypokalemia: 25-100 mg. Administer in single/divided doses.

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

How is it stored and handled?

null

How is it supplied?

bottles of 100 tablets.

Contraindications

Hypersensitivity, anuria, Addison’s disease, acute renal insufficiency, severe renal impairment (GFR < 30 mL/Min/1.73 m2), hyperkalemia, pregnancy, breastfeeding, and use with eplerenone or heparin.

Warnings and precautions

Hyperkalemia risk (avoid potassium supplements/salt substitutes). Tumorigenicity shown in rats. May cause gynecomastia (usually reversible). Caution when driving due to somnolence/dizziness.

What can be used instead?

Other Canadian products sharing ATC code C03DA01 SPIRONOLACTONE. 6 of 10 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
JAMP SPIRONOLACTONE100 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02518848
JAMP SPIRONOLACTONE25 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02518821
MINT-SPIRONOLACTONE100 MGTABLETMINT PHARMACEUTICALS INCMARKETEDDIN 02488159
MINT-SPIRONOLACTONE25 MGTABLETMINT PHARMACEUTICALS INCMARKETEDDIN 02488140
TEVA-SPIRONOLACTONE100 MGTABLETTEVA CANADA LIMITEDMARKETEDDIN 00613223
TEVA-SPIRONOLACTONE25 MGTABLETTEVA CANADA LIMITEDMARKETEDDIN 00613215
ALDACTONE 100 MG100 MGTABLETPFIZER CANADA ULCCANCELLED POST MARKETDIN 00285455
NTP-SPIRONOLACTONE100 MGTABLETNT PHARMA CANADA LTDCANCELLED PRE MARKETDIN 02347628
NTP-SPIRONOLACTONE25 MGTABLETNT PHARMA CANADA LTDCANCELLED PRE MARKETDIN 02347601

Who else supplies SPIRONOLACTONE worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. SPIRONOLACTONE appears in 137 registered pack listings across 12 markets, published on 10 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.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

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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.

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Health Canada Drug Product Database (DPD), DIN 00028606. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.