Drug Report History

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Below you will find the report version history. When a report is updated, a new version of the report is created. The report history allows you to see the changes between versions. You can select two versions of the report to compare. The fields that were changed between versions will be highlighted in yellow.

The translation of reports creates two separate versions which is why some reports may not seem to have any differences. In this case, only the language field below will be highlighted in yellow.

Version v4-FR Version v2-FR
Language French French
Date Updated 2022-10-03 2022-09-01
Drug Identification Number 02491699 02491699
Brand name HYDROMORPHONE HYDROCHLORIDE INJECTION, USP HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Common or Proper name HYDROMORPHONE HYDROCHLORIDE INJECTION, USP HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Company Name FRESENIUS KABI CANADA LTD FRESENIUS KABI CANADA LTD
Ingredients HYDROMORPHONE HYDROCHLORIDE HYDROMORPHONE HYDROCHLORIDE
Strength(s) 2MG 2MG
Dosage form(s) SOLUTION SOLUTION
Route of administration SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR
Packaging size 1mL 1mL
ATC code N02AA N02AA
ATC description OPIOIDS OPIOIDS
Reason for shortage Demand increase for the drug. Demand increase for the drug.
Anticipated start date 2022-08-08 2022-08-08
Actual start date 2022-08-08 2022-08-08
Estimated end date Unknown Unknown
Actual end date 2022-09-30
Shortage status Resolved Actual shortage
Tier 3 Status No No
Company comments This product will be placed on allocation. Contract customers will be allocated 100% of historical monthly demand. This product will be placed on allocation. Contract customers will be allocated 100% of historical monthly demand.
Health Canada comments