PERJETA DIN 02405016
Status: Marketed
Holder: HOFFMANN-LA ROCHE LIMITED
Available to quote
Health Canada record
| Active ingredient(s) | PERTUZUMAB 420 MG |
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| Dosage form | Solution |
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| Route | Intravenous |
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| Schedule | SCHEDULE D; PRESCRIPTION |
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| Class | Human |
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| ATC | L01FD02 PERTUZUMAB |
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| Original market date | 08-May-2013 |
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| Current status date | 08-May-2013 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Hoffmann-La Roche Limited — licence 100006, currently licensed, last inspection rating C (2024-06-25).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing PERTUZUMAB
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02405024 | PERJETA-HERCEPTIN | HOFFMANN-LA ROCHE LIMITED | Kit; Solution; Powder For Solution | PERTUZUMAB 420 MG; TRASTUZUMAB 440 MG | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 14288 | 2013-04-12 | New Drug Submission (NDS) | |
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