Drug · DIN 02237923
AVAPRO
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 January 22, 2025; first marketed June 22, 1998.
- Drug Identification Number (DIN)
- 02237923
- Company (DIN owner)
- Sanofi-Aventis Canada Inc.Toronto, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Irbesartan C09CA04
- Class
- Human
- Record last updated
- August 21, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| IRBESARTAN | 75 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- March 29, 2006: NOC 7855New Drug Submission (NDS) · Manufacturer name change
- September 18, 2000: NOC 1218New Drug Submission (NDS)
- June 1, 1998: NOC 2987New Drug Submission (NDS)
Recalls and safety alerts that mention it
Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “avapro”. A notice may cover another product or only some lots: read it to see what it covers.
- Sanofi-Aventis Avapro Product Recall(2021-06-14)June 14, 2021 · Drugs · Product safety · Type I
Other DINs named AVAPRO
- DIN 02237924 · Marketed
- DIN 02237925 · Marketed