Drug · DIN 02325977
OXYCODONE
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 June 10, 2009.
- Drug Identification Number (DIN)
- 02325977
- Company (DIN owner)
- Pro Doc LimiteeLaval, Quebec, Canada
- Schedule
- Narcotics (cdsa i)
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Oxycodone N02AA05
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| OXYCODONE HYDROCHLORIDE | 20 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- May 7, 2009: NOC 10197Abbreviated New Drug Submission (ANDS) · New manufacturer and product name
Other DINs named OXYCODONE
- DIN 02325950 · Cancelled Post Market
- DIN 02325969 · Cancelled Post Market