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 v7-EN Version v5-EN
Language English English
Date Updated 2020-03-24 2020-01-24
Drug Identification Number 01916971 01916971
Brand name TUSSIONEX TUSSIONEX
Common or Proper name Tussionex Tussionex
Company Name SANOFI-AVENTIS CANADA INC SANOFI-AVENTIS CANADA INC
Ingredients HYDROCODONE PHENYLTOLOXAMINE HYDROCODONE PHENYLTOLOXAMINE
Strength(s) 5MG 10MG 5MG 10MG
Dosage form(s) SUSPENSION SUSPENSION
Route of administration ORAL ORAL
Packaging size 500ml 500ml
ATC code R05DA R05DA
ATC description COUGH SUPPRESSANTS EXCL. COMB. WITH EXPECTORANTS COUGH SUPPRESSANTS EXCL. COMB. WITH EXPECTORANTS
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date 2020-01-14 2020-01-14
Actual discontinuation date 2020-02-07
Remaining supply date 2020-01-31 2020-01-31
Discontinuation status Discontinued To be discontinued
Discontinuation decision reversal no no
Information on remaining supply
Company comments
Health Canada comments