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 v6-FR Version v5-EN
Language French English
Date Updated 2018-12-28 2018-12-28
Drug Identification Number 00733059 00733059
Brand name APO-RANITIDINE TABLET 150MG APO-RANITIDINE TABLET 150MG
Common or Proper name RANITIDINE RANITIDINE
Company Name APOTEX INC APOTEX INC
Ingredients RANITIDINE RANITIDINE
Strength(s) 150MG 150MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 60 BTL 60 BTL
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 2018-10-29 2018-10-29
Remaining supply date 2018-10-29 2018-10-29
Discontinuation status Discontinued Discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments
Health Canada comments