VIZIMPRO DIN 02486032
Status: Cancelled Post Market
Holder: PFIZER CANADA ULC
Molecule: DACOMITINIB (DACOMITINIB MONOHYDRATE)
Health Canada record
| Active ingredient(s) | DACOMITINIB (DACOMITINIB MONOHYDRATE) 30 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | L01EB07 DACOMITINIB |
| Original market date | 22-Apr-2019 |
| Current status date | 24-Nov-2021 |
| Source | Health Canada DPD |
Establishment licence of the holder
Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing DACOMITINIB (DACOMITINIB MONOHYDRATE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02486024 | VIZIMPRO | PFIZER CANADA ULC | Tablet | DACOMITINIB (DACOMITINIB MONOHYDRATE) 15 MG | Cancelled Post Market |
| 02486040 | VIZIMPRO | PFIZER CANADA ULC | Tablet | DACOMITINIB (DACOMITINIB MONOHYDRATE) 45 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 21898 | 2019-02-26 | New Drug Submission (NDS) |