INSPRA 25 MG
EPLERENONE : 25 MG · DIN 02323052 · BGP PHARMA ULC
Health Canada status: MARKETED
What is INSPRA?
INSPRA 25 MG contains EPLERENONE : 25 MG. It is listed in the Health Canada Drug Product Database under DIN 02323052, held by BGP PHARMA ULC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 07-Jul-2023. 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 INSPRA used for?
Adjunct to standard therapy for NYHA class II systolic chronic heart failure, heart failure post-myocardial infarction with LV systolic dysfunction, and treatment of essential hypertension.
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
| DIN | 02323052 |
|---|---|
| Brand name | INSPRA |
| Generic / active ingredient | EPLERENONE : 25 MG |
| Manufacturer | BGP PHARMA ULC |
| Strength | 25 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | C03DA04 EPLERENONE |
| Biosimilar | No |
| Health Canada status | MARKETED |
| Status date | 07-Jul-2023 |
How is it administered?
Administered orally. For heart failure, starting dose 25 mg QD, titrated to 50 mg QD within 4 weeks. For hypertension, 50 mg QD alone or with other agents. Monitor serum potassium levels.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Not explicitly detailed in provided text (Table of Contents lists section 11, but text ends before details).
How is it supplied?
Not explicitly detailed in provided text (mentions 25 mg and 50 mg strengths).
Contraindications
Hypersensitivity; hyperkalemia; severe hepatic impairment (Child-Pugh C); eGFR <30 mL/min/1.73m2; concomitant use of potassium-sparing diuretics, potassium supplements, or strong CYP3A4 inhibitors.
Warnings and precautions
Principal risk is hyperkalemia, which can cause fatal arrhythmias. Monitor serum potassium before initiation, at 1 week, 1 month, and periodically. Risk increases with declining renal function.
What can be used instead?
Other Canadian products sharing ATC code C03DA04 EPLERENONE. 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.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| INSPRA | 50 MG | TABLET | BGP PHARMA ULC | MARKETED | DIN 02323060 |
| JAMP EPLERENONE | 25 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02543389 |
| JAMP EPLERENONE | 50 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02543397 |
| MINT-EPLERENONE | 25 MG | TABLET | MINT PHARMACEUTICALS INC | MARKETED | DIN 02471442 |
| MINT-EPLERENONE | 50 MG | TABLET | MINT PHARMACEUTICALS INC | MARKETED | DIN 02471450 |
| APO-EPLERENONE | 25 MG | TABLET | APOTEX INC | APPROVED | DIN 02465019 |
| APO-EPLERENONE | 50 MG | TABLET | APOTEX INC | APPROVED | DIN 02465027 |
| GD-EPLERENONE | 25 MG | TABLET | GENMED A DIVISION OF PFIZER CANADA ULC | CANCELLED PRE MARKET | DIN 02441543 |
| GD-EPLERENONE | 50 MG | TABLET | GENMED A DIVISION OF PFIZER CANADA ULC | CANCELLED PRE MARKET | DIN 02441578 |
Who else supplies EPLERENONE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. EPLERENONE appears in 218 registered pack listings across 13 markets, published on 11 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.
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.