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.

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Version v3-FR Version v2-FR
Language French French
Date Updated 2019-04-11 2019-04-11
Drug Identification Number 02022133 02022133
Brand name TEVA-FAMOTIDINE TEVA-FAMOTIDINE
Common or Proper name FAMOTIDINE FAMOTIDINE
Company Name TEVA CANADA LIMITED TEVA CANADA LIMITED
Ingredients FAMOTIDINE FAMOTIDINE
Strength(s) 20MG 20MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 500 500
ATC code A02BA A02BA
ATC description DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD) DRUGS FOR PEPTIC ULCER AND GASTROESOPHAGEAL REFLUX DISEASE (GERD)
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date
Actual discontinuation date 2019-01-09 2019-01-09
Remaining supply date 2019-02-28 2019-02-28
Discontinuation status Discontinued Discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments
Health Canada comments