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 v3-EN Version v3-EN
Language English English
Date Updated 2020-07-23 2020-07-23
Drug Identification Number 00740756 00740756
Brand name RANITIDINE RANITIDINE
Common or Proper name RANITIDINE - 300 RANITIDINE - 300
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients RANITIDINE RANITIDINE
Strength(s) 300MG 300MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL ORAL ORAL
Packaging size 100 100
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 shortage Other (Please describe in comments) Other (Please describe in comments)
Anticipated start date
Actual start date 2020-07-22 2020-07-22
Estimated end date Unknown Unknown
Actual end date
Shortage status Actual shortage Actual shortage
Company comments Regulatory issues, Enjeux règlementaires Regulatory issues, Enjeux règlementaires
Health Canada comments