Drug Report History

Return to report

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 v9-EN Version v1-EN
Language English English
Date Updated 2023-03-07 2023-01-04
Drug Identification Number 00897639 00897639
Brand name ISOPROTERENOL HYDROCHLORIDE INJECTION USP ISOPROTERENOL HYDROCHLORIDE INJECTION USP
Common or Proper name Isoproterenol Isoproterenol
Company Name SANDOZ CANADA INCORPORATED SANDOZ CANADA INCORPORATED
Ingredients ISOPROTERENOL HYDROCHLORIDE ISOPROTERENOL HYDROCHLORIDE
Strength(s) 0.2MG 0.2MG
Dosage form(s) SOLUTION SOLUTION
Route of administration SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR SUBCUTANEOUS INTRAVENOUS INTRAMUSCULAR
Packaging size 10 x 1ML Ampoules 10 x 1ML Ampoules
ATC code C01CA C01CA
ATC description CARDIAC STIMULANTS EXCL. CARDIAC GLYCOSIDES CARDIAC STIMULANTS EXCL. CARDIAC GLYCOSIDES
Reason for shortage Shortage of an active ingredient. Disruption of the manufacture of the drug.
Anticipated start date 2023-01-01
Actual start date 2023-01-18 2023-01-01
Estimated end date 2023-03-10 2023-03-31
Actual end date 2023-03-06
Shortage status Resolved Actual shortage
Tier 3 Status No No
Company comments
Health Canada comments