MVASI DIN 02470748
Status: Marketed
Holder: AMGEN CANADA INC
Available to quote
Health Canada record
| Active ingredient(s) | BEVACIZUMAB 25 MG |
|---|
| Dosage form | Solution |
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| Route | Intravenous |
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| Schedule | SCHEDULE D; PRESCRIPTION |
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| Class | Human |
|---|
| ATC | L01FG01 BEVACIZUMAB |
|---|
| Original market date | 01-Aug-2019 |
|---|
| Current status date | 01-Aug-2019 |
|---|
| Source | Health Canada DPD |
|---|
Establishment licence of the holder
Amgen Canada Inc — licence 100048, currently licensed, last inspection rating C (2023-03-01).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing BEVACIZUMAB
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02522160 | ABEVMY | BIOCON BIOLOGICS CANADA INC | Solution | BEVACIZUMAB 400 MG | Marketed |
| 02522179 | ABEVMY | BIOCON BIOLOGICS CANADA INC | Solution | BEVACIZUMAB 100 MG | Marketed |
| 02270994 | AVASTIN | HOFFMANN-LA ROCHE LIMITED | Solution | BEVACIZUMAB 25 MG | Marketed |
| 02522829 | AYBINTIO | SAMSUNG BIOEPIS CO., LTD | Solution | BEVACIZUMAB 100 MG | Marketed |
| 02522837 | AYBINTIO | SAMSUNG BIOEPIS CO., LTD | Solution | BEVACIZUMAB 400 MG | Marketed |
| 02520729 | BAMBEVI | APOTEX INC | Solution | BEVACIZUMAB 100 MG | Marketed |
| 02520737 | BAMBEVI | APOTEX INC | Solution | BEVACIZUMAB 400 MG | Marketed |
| 02567865 | BEVQOLVA | CURATEQ BIOLOGICS PRIVATE LIMITED | Solution | BEVACIZUMAB 400 MG | Approved |
| 02567830 | BEVQOLVA | CURATEQ BIOLOGICS PRIVATE LIMITED | Solution | BEVACIZUMAB 100 MG | Approved |
| 02470756 | MVASI | AMGEN CANADA INC | Solution | BEVACIZUMAB 25 MG | Marketed |
| 02534177 | VEGZELMA | CELLTRION INC. | Solution | BEVACIZUMAB 100 MG | Marketed |
| 02534185 | VEGZELMA | CELLTRION INC. | Solution | BEVACIZUMAB 400 MG | Marketed |
| 02489430 | ZIRABEV | PFIZER CANADA ULC | Solution | BEVACIZUMAB 100 MG | Marketed |
| 02489449 | ZIRABEV | PFIZER CANADA ULC | Solution | BEVACIZUMAB 400 MG | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 20799 | 2018-04-30 | New Drug Submission (NDS) | |
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