ZONOVATE DIN 02435233
Status: Dormant
Holder: NOVO NORDISK CANADA INC
Health Canada record
| Active ingredient(s) | TUROCTOCOG ALFA 3000 UNIT |
|---|
| Dosage form | Powder For Solution; Kit |
|---|
| Route | Intravenous |
|---|
| Schedule | SCHEDULE D |
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| Class | Human |
|---|
| ATC | B02BD02 COAGULATION FACTOR VIII |
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| Original market date | 23-Mar-2018 |
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| Current status date | 24-Jul-2026 |
|---|
| Source | Health Canada DPD |
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Establishment licence of the holder
Novo Nordisk Canada Inc — licence 100175, currently licensed, last inspection rating C (2023-02-13).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing TUROCTOCOG ALFA
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02435187 | ZONOVATE | NOVO NORDISK CANADA INC | Kit; Powder For Solution | TUROCTOCOG ALFA 250 UNIT | Dormant |
| 02435195 | ZONOVATE | NOVO NORDISK CANADA INC | Powder For Solution; Kit | TUROCTOCOG ALFA 500 UNIT | Dormant |
| 02435217 | ZONOVATE | NOVO NORDISK CANADA INC | Powder For Solution; Kit | TUROCTOCOG ALFA 1500 UNIT | Dormant |
| 02435225 | ZONOVATE | NOVO NORDISK CANADA INC | Powder For Solution; Kit | TUROCTOCOG ALFA 2000 UNIT | Dormant |
| 02435209 | ZONOVATE | NOVO NORDISK CANADA INC | Powder For Solution; Kit | TUROCTOCOG ALFA 1000 UNIT | Dormant |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 16408 | 2014-12-08 | New Drug Submission (NDS) | |
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