AURO-REPAGLINIDE 0.5 MG
REPAGLINIDE : 0.5 MG · DIN 02424258 · AURO PHARMA INC
Health Canada status: MARKETED
What is AURO-REPAGLINIDE?
AURO-REPAGLINIDE 0.5 MG contains REPAGLINIDE : 0.5 MG. It is listed in the Health Canada Drug Product Database under DIN 02424258, held by AURO PHARMA INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 30-Apr-2014. 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
| DIN | 02424258 |
|---|---|
| Brand name | AURO-REPAGLINIDE |
| Generic / active ingredient | REPAGLINIDE : 0.5 MG |
| Manufacturer | AURO PHARMA INC |
| Strength | 0.5 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | A10BX02 REPAGLINIDE |
| AHFS class | 68:20.16 |
| Biosimilar | No |
| Health Canada status | MARKETED |
| Status date | 30-Apr-2014 |
| Original market date | 2014-04-30 00:00:00 |
What can be used instead?
Other Canadian products sharing ATC code A10BX02 REPAGLINIDE. 12 of 27 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 |
|---|---|---|---|---|---|
| AURO-REPAGLINIDE | 1 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02424266 |
| AURO-REPAGLINIDE | 2 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02424274 |
| JAMP REPAGLINIDE | 0.5 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02354926 |
| JAMP REPAGLINIDE | 1 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02354934 |
| JAMP REPAGLINIDE | 2 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02354942 |
| REPAGLINIDE | 0.5 MG | TABLET | PRO DOC LIMITEE | MARKETED | DIN 02415968 |
| REPAGLINIDE | 1 MG | TABLET | PRO DOC LIMITEE | MARKETED | DIN 02415976 |
| REPAGLINIDE | 2 MG | TABLET | PRO DOC LIMITEE | MARKETED | DIN 02415984 |
| SANDOZ REPAGLINIDE | 0.5 MG | TABLET | SANDOZ CANADA INCORPORATED | MARKETED | DIN 02357453 |
| SANDOZ REPAGLINIDE | 1 MG | TABLET | SANDOZ CANADA INCORPORATED | MARKETED | DIN 02357461 |
Who else supplies REPAGLINIDE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. REPAGLINIDE appears in 103 registered pack listings across 11 markets, published on 8 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.