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 v11-FR Version v10-EN
Language French English
Date Updated 2017-05-24 2017-05-24
Drug Identification Number 02292378 02292378
Brand name APO-PRAMIPEXOLE APO-PRAMIPEXOLE
Common or Proper name PRAMIPEXOLE PRAMIPEXOLE
Company Name APOTEX INC APOTEX INC
Ingredients PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
Strength(s) 0.25MG 0.25MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 BTL 100 BTL
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 2017-04-19 2017-04-19
Estimated end date 2017-05-26 2017-05-26
Actual end date 2017-05-19 2017-05-19
Shortage status Resolved Resolved
Tier 3 Status No No
Company comments
Health Canada comments