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 v6-EN Version v2-FR
Language English French
Date Updated 2019-11-30 2019-11-20
Drug Identification Number 00060208 00060208
Brand name 0.9% SODIUM CHLORIDE INJECTION, USP 0.9% SODIUM CHLORIDE INJECTION, USP
Common or Proper name 0.9% SODIUM CHLORIDE INJECTION, USP 0.9% SODIUM CHLORIDE INJECTION, USP
Company Name BAXTER CORPORATION BAXTER CORPORATION
Ingredients SODIUM CHLORIDE SODIUM CHLORIDE
Strength(s) 900MG 900MG
Dosage form(s) SOLUTION SOLUTION
Route of administration INTRAVENOUS INTRAVENOUS
Packaging size 25 mL (JB1300) 25 mL (JB1300)
ATC code B05XA B05XA
ATC description I.V. SOLUTION ADDITIVES I.V. SOLUTION ADDITIVES
Reason for shortage Demand increase for the drug. Demand increase for the drug.
Anticipated start date 2019-11-20 2019-11-20
Actual start date 2019-11-20 2019-11-20
Estimated end date 2019-11-29 2019-11-29
Actual end date 2019-11-29
Shortage status Resolved Anticipated shortage
Tier 3 Status No No
Company comments
Health Canada comments