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 v5-FR Version v4-EN
Language French English
Date Updated 2019-01-03 2019-01-03
Drug Identification Number 02292394 02292394
Brand name APO-PRAMIPEXOLE APO-PRAMIPEXOLE
Common or Proper name PRAMIPEXOLE 1.0MG PRAMIPEXOLE 1.0MG
Company Name APOTEX INC APOTEX INC
Ingredients PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
Strength(s) 1.0MG 1.0MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100BTL 100BTL
ATC code N04BC N04BC
ATC description DOPAMINERGIC AGENTS DOPAMINERGIC AGENTS
Reason for shortage Disruption of the manufacture of the drug. Disruption of the manufacture of the drug.
Anticipated start date
Actual start date 2018-11-26 2018-11-26
Estimated end date 2019-01-25 2019-01-25
Actual end date 2019-01-02 2019-01-02
Shortage status Resolved Resolved
Tier 3 Status No No
Company comments
Health Canada comments