Drug · DIN 02395681
FENTANYL PATCH
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 November 1, 2019; first marketed November 22, 2012.
- Drug Identification Number (DIN)
- 02395681
- Company (DIN owner)
- Pro Doc LimiteeLaval, Quebec, Canada
- Schedule
- Narcotics (cdsa i)
- Dosage form
- Patch
- Route
- Transdermal
- Therapeutic class (ATC)
- Fentanyl N02AB03
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| FENTANYL | 75 MCG | HOUR |
Notices of Compliance
Health Canada approvals that name this DIN.
- November 1, 2012: NOC 13797Abbreviated New Drug Submission (ANDS) · New manufacturer and product name
Other DINs named FENTANYL PATCH
- DIN 02395657 · Cancelled Post Market
- DIN 02395665 · Cancelled Post Market
- DIN 02395673 · Cancelled Post Market
- DIN 02395703 · Cancelled Post Market