Discontinuation report ARICEPT RDT
| Report ID | 137465 |
| Drug Identification Number | 02269457 |
| Brand name | ARICEPT RDT |
| Common or Proper name | Aricept |
| Company Name | PFIZER CANADA ULC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | DONEPEZIL HYDROCHLORIDE |
| Strength(s) | 5MG |
| Dosage form(s) | TABLET (ORALLY DISINTEGRATING) |
| Route of administration | ORAL ORAL |
| Packaging size | 2x14 Blisters |
| ATC code | N06DA |
| ATC description | ANTI-DEMENTIA DRUGS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | 2022-03-01 |
| Actual discontinuation date | |
| Remaining supply date | 2022-03-01 |
| Discontinuation status | To be discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| Company comments | Aricept 5mg and 10mg Tabs in 30 count bottles remain available. |
| Health Canada comments | |
| Tier 3 Status | No |
| Contact Address | 17300 TRANS-CANADA HIGHWAY KIRKLAND, QUEBEC CANADA H9J 2M5 |
| Company contact information | Customer Service / service à la clientèle : 1-888-999-8750 Email / courriel: PharmaCustomerServiceDept@pfizer.com |
Version History
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| Version Number | Date Updated | Language | |
|---|---|---|---|
| v1 | 2021-04-14 | English | Compare |
| v2 | 2021-04-14 | French | Compare |
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