Drug · DIN 02367203
AVA-RISPERIDONE
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 August 21, 2014; first marketed August 18, 2011.
- Drug Identification Number (DIN)
- 02367203
- Company (DIN owner)
- Avanstra IncCalgary, Alberta, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Risperidone N05AX08
- Class
- Human
- Record last updated
- June 18, 2026
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| RISPERIDONE | 1.0 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- May 6, 2011: NOC 12320Abbreviated New Drug Submission (ANDS) · New manufacturer and product name
Other DINs named AVA-RISPERIDONE
- DIN 02364344 · Cancelled Post Market
- DIN 02367173 · Cancelled Post Market
- DIN 02367181 · Cancelled Post Market
- DIN 02367211 · Cancelled Post Market
- DIN 02367238 · Cancelled Post Market
- DIN 02367246 · Cancelled Post Market