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 v5-EN Version v2-FR
Language English French
Date Updated 2021-06-29 2021-05-07
Drug Identification Number 02331616 02331616
Brand name BUPROPION SR BUPROPION SR
Common or Proper name BUPROPION SR BUPROPION SR
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE
Strength(s) 100MG 100MG
Dosage form(s) TABLET (EXTENDED-RELEASE) TABLET (EXTENDED-RELEASE)
Route of administration ORAL ORAL ORAL ORAL
Packaging size 60 60
ATC code N06AX N06AX
ATC description ANTIDEPRESSANTS ANTIDEPRESSANTS
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date 2021-06-30 2021-06-30
Actual discontinuation date 2021-06-28
Remaining supply date 2021-10-31 2021-10-31
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