Discontinuation report HYDROMORPHONE HYDROCHLORIDE INJECTION USP
| Report ID | 268504 |
| Drug Identification Number | 02382636 |
| Brand name | HYDROMORPHONE HYDROCHLORIDE INJECTION USP |
| Common or Proper name | HYDROMORPHONE HYDROCHLORIDE INJECTION USP |
| Company Name | PFIZER CANADA ULC |
| Market Status | MARKETED |
| Active Ingredient(s) | HYDROMORPHONE HYDROCHLORIDE |
| Strength(s) | 10MG |
| Dosage form(s) | SOLUTION |
| Route of administration | SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR |
| Packaging size | 10 X 5ML VIAL |
| ATC code | N02AA |
| ATC description | OPIOIDS |
| Reason for discontinuation | Business reasons |
| Anticipated discontinuation date | |
| Actual discontinuation date | 2025-10-01 |
| Remaining supply date | |
| Discontinuation status | Discontinued |
| Discontinuation decision reversal | No |
| Information on remaining supply | |
| 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 | |
|---|---|---|---|
| v2 | 2025-10-02 | French | Compare |
| v1 | 2025-10-02 | English | Compare |
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