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 v8-EN Version v7-FR
Language English French
Date Updated 2024-03-14 2024-03-13
Drug Identification Number 02424096 02424096
Brand name AURO-PRAMIPEXOLE AURO-PRAMIPEXOLE
Common or Proper name AURO-PRAMIPEXOLE AURO-PRAMIPEXOLE
Company Name AURO PHARMA INC AURO PHARMA INC
Ingredients PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
Strength(s) 1MG 1MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL ORAL ORAL
Packaging size 100's 100's
ATC code N04BC N04BC
ATC description DOPAMINERGIC AGENTS DOPAMINERGIC AGENTS
Reason for shortage Demand increase for the drug. Demand increase for the drug.
Anticipated start date
Actual start date 2024-01-29 2024-01-29
Estimated end date 2024-03-15 2024-03-15
Actual end date 2024-03-13 2024-03-13
Shortage status Resolved Actual shortage
Tier 3 Status No No
Company comments
Health Canada comments