APOQUEL DIN 02427893
Status: Marketed
Holder: ZOETIS CANADA INC
Health Canada record
| Active ingredient(s) | OCLACITINIB (OCLACITINIB MALEATE) 5.4 MG |
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| Dosage form | Tablet |
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| Route | Oral |
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| Schedule | PRESCRIPTION |
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| Class | Veterinary |
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| ATC | |
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| Original market date | 10-Mar-2016 |
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| Current status date | 10-Mar-2016 |
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| Source | Health Canada DPD |
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Establishment licence of the holder
Zoetis Canada Inc — licence 102076, currently licensed, last inspection rating C (2023-10-05).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing OCLACITINIB (OCLACITINIB MALEATE)
| DIN | Product | Company | Form | Strength | Status |
|---|
| 02427885 | APOQUEL | ZOETIS CANADA INC | Tablet | OCLACITINIB (OCLACITINIB MALEATE) 3.6 MG | Marketed |
| 02427907 | APOQUEL | ZOETIS CANADA INC | Tablet | OCLACITINIB (OCLACITINIB MALEATE) 16 MG | Marketed |
| 02530651 | APOQUEL | ZOETIS CANADA INC | Tablet (Chewable) | OCLACITINIB (OCLACITINIB MALEATE) 3.6 MG | Marketed |
| 02530678 | APOQUEL | ZOETIS CANADA INC | Tablet (Chewable) | OCLACITINIB (OCLACITINIB MALEATE) 5.4 MG | Marketed |
| 02530686 | APOQUEL | ZOETIS CANADA INC | Tablet (Chewable) | OCLACITINIB (OCLACITINIB MALEATE) 16 MG | Marketed |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|
| 29554 | 2022-11-28 | Supplement to a New Drug Submission (SNDS) | Addition of drug substance manufacturing and testing site |
| 15811 | 2014-07-15 | New Drug Submission (NDS) | |
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