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 v4-FR Version v2-FR
Language French French
Date Updated 2017-07-26 2017-05-08
Drug Identification Number 00434388 00434388
Brand name DIAZEPAM 10TAB 10MG DIAZEPAM 10TAB 10MG
Common or Proper name DIAZEPAM DIAZEPAM
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients DIAZEPAM DIAZEPAM
Strength(s) 10MG 10MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 100
ATC code N05BA N05BA
ATC description ANXIOLYTICS ANXIOLYTICS
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date 2017-07-31 2017-07-31
Actual discontinuation date 2017-07-26
Remaining supply date 2019-09-30 2019-09-30
Discontinuation status To be discontinued To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments
Health Canada comments