Drug · DIN 00629359
TEVA-PROFEN
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 23, 2025; first marketed December 31, 1985.
- Drug Identification Number (DIN)
- 00629359
- Company (DIN owner)
- Teva Canada LimitedToronto, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Ibuprofen M01AE01
- Class
- Human
- Record last updated
- July 30, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| IBUPROFEN | 600 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- December 19, 2013: NOC 15038New Drug Submission (NDS) · Manufacturer name change