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 v10-EN Version v5-EN
Language English English
Date Updated 2019-06-26 2019-06-04
Drug Identification Number 02310228 02310228
Brand name PRO-FENO-SUPER - 100 PRO-FENO-SUPER - 100
Common or Proper name FENOFIBRATE FENOFIBRATE
Company Name PRO DOC LIMITEE PRO DOC LIMITEE
Ingredients FENOFIBRATE FENOFIBRATE
Strength(s) 100MG 100MG
Dosage form(s) TABLET TABLET
Route of administration ORAL ORAL
Packaging size 100 100
ATC code C10AB C10AB
ATC description LIPID MODIFYING AGENTS, PLAIN LIPID MODIFYING AGENTS, PLAIN
Reason for shortage Other (Please describe in comments) Delay in shipping of the drug.
Anticipated start date
Actual start date 2019-06-04 2019-06-04
Estimated end date Unknown
Actual end date 2019-06-25
Shortage status Resolved Anticipated shortage
Tier 3 Status No No
Company comments Has been discontinued Est maintenant discontinué Looking for an alternate source of supply. Recherche d'une source d'approvisionnement alternative
Health Canada comments