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 2018-09-07 2018-09-07
Drug Identification Number 00262005 00262005
Brand name SODIUM CHLORIDE INJECTION USP SODIUM CHLORIDE INJECTION USP
Common or Proper name SODIUM CHLORIDE SODIUM CHLORIDE
Company Name PFIZER CANADA ULC PFIZER CANADA ULC
Ingredients SODIUM CHLORIDE SODIUM CHLORIDE
Strength(s) 146MG 146MG
Dosage form(s) SOLUTION SOLUTION
Route of administration INTRAVENOUS INTRAVENOUS
Packaging size 25x20mL 25x20mL
ATC code B05XA B05XA
ATC description I.V. SOLUTION ADDITIVES I.V. SOLUTION ADDITIVES
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date
Actual discontinuation date 2018-09-06 2018-09-06
Remaining supply date 2018-09-06 2018-09-06
Discontinuation status Discontinued Discontinued
Discontinuation decision reversal no no
Information on remaining supply
Company comments
Health Canada comments