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 v5-FR Version v4-EN
Language French English
Date Updated 2019-08-28 2019-08-28
Drug Identification Number 02391090 02391090
Brand name LABETALOL HYDROCHLORIDE INJECTION USP LABETALOL HYDROCHLORIDE INJECTION USP
Common or Proper name Labetalol Labetalol
Company Name PFIZER CANADA ULC PFIZER CANADA ULC
Ingredients LABETALOL HYDROCHLORIDE LABETALOL HYDROCHLORIDE
Strength(s) 5MG 5MG
Dosage form(s) SOLUTION SOLUTION
Route of administration INTRAVENOUS INTRAVENOUS
Packaging size 50x1mL Amp 50x1mL Amp
ATC code C07AG C07AG
ATC description BETA BLOCKING AGENTS BETA BLOCKING AGENTS
Reason for shortage Demand increase for the drug. Demand increase for the drug.
Anticipated start date
Actual start date 2019-07-15 2019-07-15
Estimated end date
Actual end date 2019-08-27 2019-08-27
Shortage status Resolved Resolved
Tier 3 Status No No
Company comments
Health Canada comments