Discontinuation report ZITHROMAX
| Report ID | 264088 |
| Drug Identification Number | 02223724 |
| Brand name | ZITHROMAX |
| Common or Proper name | ZITHROMAX |
| Company Name | PFIZER CANADA ULC |
| Market Status | CANCELLED POST MARKET |
| Active Ingredient(s) | AZITHROMYCIN |
| Strength(s) | 200MG |
| Dosage form(s) | POWDER FOR SUSPENSION |
| Route of administration | ORAL ORAL |
| Packaging size | 15 ML & 22.5 ml BOTTLE |
| ATC code | J01FA |
| ATC description | MACROLIDES, LINCOSAMIDES AND STREPTOGRAMINS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2025-08-01 |
| Remaining supply date | 2022-11-29 |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | Out of stock |
| Company comments | |
| 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 | |
|---|---|---|---|
| v3 | 2025-08-02 | English | Compare |
| v2 | 2025-08-01 | French | Compare |
| v1 | 2025-08-01 | English | Compare |
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