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 v3-EN Version v1-EN
Language English English
Date Updated 2019-06-26 2019-06-25
Drug Identification Number 02311011 02311011
Brand name PRO-HYDROXYQUINE - 200 PRO-HYDROXYQUINE - 200
Common or Proper name PRO-HYDROXYQUINE - 200 PRO-HYDROXYQUINE - 200
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients HYDROXYCHLOROQUINE SULFATE HYDROXYCHLOROQUINE SULFATE
Strength(s) 200MG 200MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 100
ATC code P01BA P01BA
ATC description ANTIMALARIALS ANTIMALARIALS
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date
Actual discontinuation date 2019-06-25 2019-06-25
Remaining supply date 2020-11-30 2020-11-30
Discontinuation status Discontinued To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments
Health Canada comments