Drug · DIN 01927779
STEMETIL
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 30, 2007; first marketed December 31, 1957.
- Drug Identification Number (DIN)
- 01927779
- Company (DIN owner)
- Sanofi-Aventis Canada Inc.Toronto, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Solution
- Route
- Intramuscular; Intravenous
- Therapeutic class (ATC)
- Prochlorperazine N05AB04
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE) | 5 MG | ML |
Notices of Compliance
Health Canada approvals that name this DIN.
- May 30, 2006: NOC 7988New Drug Submission (NDS) · Manufacturer name change
- November 14, 2000: NOC 1377New Drug Submission (NDS)
Other DINs named STEMETIL
- DIN 01927795 · Cancelled Post Market