LATUDA 120 MG
LURASIDONE HYDROCHLORIDE : 120 MG · DIN 02387786 · SUMITOMO PHARMA CANADA, INC.
Health Canada status: CANCELLED POST MARKET
What is LATUDA?
LATUDA 120 MG contains LURASIDONE HYDROCHLORIDE : 120 MG. It is listed in the Health Canada Drug Product Database under DIN 02387786, held by SUMITOMO PHARMA CANADA, INC., supplied as TABLET for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 19-Aug-2025. 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 | 02387786 |
|---|---|
| Brand name | LATUDA |
| Generic / active ingredient | LURASIDONE HYDROCHLORIDE : 120 MG |
| Manufacturer | SUMITOMO PHARMA CANADA, INC. |
| Strength | 120 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | N05AE05 LURASIDONE |
| AHFS class | 28:16.08.04 |
| Biosimilar | No |
| Health Canada status | CANCELLED POST MARKET |
| Status date | 19-Aug-2025 |
| Original market date | 2012-09-06 00:00:00 |
What can be used instead?
Other Canadian products sharing ATC code N05AE05 LURASIDONE. 33 of 40 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-LURASIDONE | 120 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02514036 |
| AURO-LURASIDONE | 20 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02513986 |
| AURO-LURASIDONE | 40 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02513994 |
| AURO-LURASIDONE | 60 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02514001 |
| AURO-LURASIDONE | 80 MG | TABLET | AURO PHARMA INC | MARKETED | DIN 02514028 |
| JAMP LURASIDONE | 120 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02516470 |
| JAMP LURASIDONE | 20 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02516438 |
| JAMP LURASIDONE | 40 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02516446 |
| JAMP LURASIDONE | 60 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02516454 |
| JAMP LURASIDONE | 80 MG | TABLET | JAMP PHARMA CORPORATION | MARKETED | DIN 02516462 |
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.