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.

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Version v10-EN Version v10-EN
Language English English
Date Updated 2022-06-17 2022-06-17
Drug Identification Number 02491680 02491680
Brand name HYDROMORPHONE HYDROCHLORIDE INJECTION, USP HYDROMORPHONE HYDROCHLORIDE INJECTION, USP
Common or Proper name HYDROmorphone Hydrochloride Injection, USP 10mg/mL SD Vial 1mL HYDROmorphone Hydrochloride Injection, USP 10mg/mL SD Vial 1mL
Company Name FRESENIUS KABI CANADA LTD FRESENIUS KABI CANADA LTD
Ingredients HYDROMORPHONE HYDROCHLORIDE HYDROMORPHONE HYDROCHLORIDE
Strength(s) 10MG 10MG
Dosage form(s) SOLUTION SOLUTION
Route of administration SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR
Packaging size 10 10
ATC code N02AA N02AA
ATC description OPIOIDS OPIOIDS
Reason for shortage Disruption of the manufacture of the drug. Disruption of the manufacture of the drug.
Anticipated start date 2022-04-01 2022-04-01
Actual start date 2022-04-01 2022-04-01
Estimated end date 2022-06-20 2022-06-20
Actual end date 2022-06-16 2022-06-16
Shortage status Resolved Resolved
Tier 3 Status No No
Company comments Supply interruption due to production delays. Supply interruption due to production delays.
Health Canada comments