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-FR
Language English French
Date Updated 2019-06-04 2019-06-03
Drug Identification Number 02225158 02225158
Brand name SUPREFACT SUPREFACT
Common or Proper name Suprefact Suprefact
Company Name CHEPLAPHARM ARZNEIMITTEL GMBH CHEPLAPHARM ARZNEIMITTEL GMBH
Ingredients BUSERELIN BUSERELIN
Strength(s) 1MG 1MG
Dosage form(s) SOLUTION SOLUTION
Route of administration NASAL NASAL
Packaging size 2 2
ATC code L02AE L02AE
ATC description HORMONES AND RELATED AGENTS HORMONES AND RELATED AGENTS
Reason for shortage Other (Please describe in comments) Other (Please describe in comments)
Anticipated start date 2019-05-10 2019-05-10
Actual start date
Estimated end date 2019-06-28 2019-06-28
Actual end date 2019-06-03 2019-06-03
Shortage status Resolved Actual shortage
Tier 3 Status No No
Company comments Manufacturing Delay. The anticipated availability dates represent estimated availabilities at the main Sanofi warehouse. Availability dates at a customer’s usual distributor warehouse may vary. Pharmacies are invited to communicate with their preferred distributor to obtain the product availability date. Patients should validate the availability of the product with their respective pharmacy. Manufacturing Delay. The anticipated availability dates represent estimated availabilities at the main Sanofi warehouse. Availability dates at a customer’s usual distributor warehouse may vary. Pharmacies are invited to communicate with their preferred distributor to obtain the product availability date. Patients should validate the availability of the product with their respective pharmacy.
Health Canada comments