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 v9-FR Version v8-EN
Language French English
Date Updated 2019-01-08 2019-01-08
Drug Identification Number 02331616 02331616
Brand name BUPROPION SR BUPROPION SR
Common or Proper name BUPROPION BUPROPION
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
Packaging size 60 60
ATC code N06AX N06AX
ATC description ANTIDEPRESSANTS ANTIDEPRESSANTS
Reason for shortage Demand increase for the drug. Demand increase for the drug.
Anticipated start date 2019-01-07 2019-01-07
Actual start date
Estimated end date
Actual end date 2019-01-07 2019-01-07
Shortage status Resolved Resolved
Tier 3 Status No No
Company comments
Health Canada comments