Drug · DIN 02443759
VIIBRYD
STARTER KIT (10 MG AND 20 MG TABLETS)
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 July 20, 2023; first marketed July 6, 2018.
- Drug Identification Number (DIN)
- 02443759
- Company (DIN owner)
- AbbVie CorporationSaint-Laurent, Quebec, Canada
- Schedule
- Prescription
- Dosage form
- Kit; Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Vilazodone N06AX24
- Class
- Human
- Record last updated
- September 14, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| VILAZODONE HYDROCHLORIDE | 10 MG | |
| VILAZODONE HYDROCHLORIDE | 20 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- November 21, 2022: NOC 29513New Drug Submission (NDS) · Administrative: Merger/Buy-out
- July 16, 2015: NOC 17096New Drug Submission (NDS)
Other DINs named VIIBRYD
- DIN 02443724 · Marketed
- DIN 02443732 · Marketed
- DIN 02443740 · Marketed
- DIN 02443767 · Cancelled Pre Market