STEMETIL DIN 01927779
Status: Cancelled Post Market
Holder: SANOFI-AVENTIS CANADA INC
Health Canada record
| Active ingredient(s) | PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE) 5 MG |
|---|---|
| Dosage form | Solution |
| Route | Intramuscular; Intravenous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | N05AB04 PROCHLORPERAZINE |
| Original market date | 31-Dec-1957 |
| Current status date | 30-Jan-2007 |
| Source | Health Canada DPD |
Establishment licence of the holder
sanofi-aventis Canada Inc. — licence 101470, currently licensed, last inspection rating C (2026-02-17).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00753645 | PMS PROCHLORPERAZINE INJ 5MG/ML | PHARMASCIENCE INC | Solution | PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE) 5 MG | Cancelled Post Market |
| 00789747 | PROCHLORPERAZINE MESYLATE INJ 5MG/ML | SANDOZ CANADA INCORPORATED | Liquid | PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE) 5 MG | Cancelled Post Market |
| 01927787 | STEMETIL LIQ 5MG/5ML | AVENTIS PHARMA INC | Syrup | PROCHLORPERAZINE (PROCHLORPERAZINE MESYLATE) 5 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 7988 | 2006-05-30 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 1377 | 2000-11-14 | New Drug Submission (NDS) |