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 v6-EN
Language English English
Date Updated 2017-03-27 2017-03-24
Drug Identification Number 02326795 02326795
Brand name AMLODIPINE AMLODIPINE
Common or Proper name AMLODIPINE AMLODIPINE
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients AMLODIPINE AMLODIPINE
Strength(s) 2.5MG 2.5MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 100
ATC code C08CA C08CA
ATC description SELECTIVE CALC.CHANNEL BLOCK. W/MAINLY VASC. EFF. SELECTIVE CALC.CHANNEL BLOCK. W/MAINLY VASC. EFF.
Reason for shortage Delay in shipping of the drug. Delay in shipping of the drug.
Anticipated start date 2017-03-28 2017-03-23
Actual start date
Estimated end date 2017-06-01 2017-06-01
Actual end date
Shortage status Anticipated shortage Actual shortage
Tier 3 Status No No
Company comments
Health Canada comments