Drug · DIN 02413361
LATUDA
FILM-COATED TABLET
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since June 30, 2026; first marketed March 14, 2014.
- Drug Identification Number (DIN)
- 02413361
- Company (DIN owner)
- Sumitomo Pharma Canada, Inc.Mississauga, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Lurasidone N05AE05
- Class
- Human
- Record last updated
- August 6, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| LURASIDONE HYDROCHLORIDE | 60 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- January 19, 2024: NOC 32558New Drug Submission (NDS) · Administrative: Manufacturer Name Change
- October 10, 2013: NOC 14804Supplement to a New Drug Submission (SNDS) · New strength and manufacturing site for that strength
Other DINs named LATUDA
- DIN 02387751 · Cancelled Post Market
- DIN 02387778 · Cancelled Post Market
- DIN 02387786 · Cancelled Post Market
- DIN 02422050 · Cancelled Post Market