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Version v6-EN Version v2-FR
Language English French
Date Updated 2025-05-12 2025-04-03
Drug Identification Number 02392453 02392453
Brand name HEPARIN SODIUM INJECTION, USP HEPARIN SODIUM INJECTION, USP
Common or Proper name HEPARIN SODIUM INJECTION, USP HEPARIN SODIUM INJECTION, USP
Company Name FRESENIUS KABI CANADA LTD FRESENIUS KABI CANADA LTD
Ingredients HEPARIN SODIUM HEPARIN SODIUM
Strength(s) 10000UNIT 10000UNIT
Dosage form(s) SOLUTION SOLUTION
Route of administration SUBCUTANEOUS INTRAVENOUS SUBCUTANEOUS INTRAVENOUS SUBCUTANEOUS INTRAVENOUS SUBCUTANEOUS INTRAVENOUS
Packaging sizes (GTIN) (See additional packaging sizes) (See additional packaging sizes)
Additional packaging sizes 0.5mL 0.5mL
ATC code B01AB B01AB
ATC description ANTITHROMBOTIC AGENTS ANTITHROMBOTIC AGENTS
Reason for shortage Disruption of the manufacture of the drug. Disruption of the manufacture of the drug.
Anticipated start date
Actual start date 2025-04-30 2025-04-30
Estimated end date 2025-05-22 2025-06-02
Actual end date 2025-05-22
Shortage status Actual shortage Anticipated shortage
Tier 3 Status No No
Company comments Fresenius Kabi Canada is pleased to advise that this product will be made available earlier than originally communicated. It will be available at Ontario distribution centres by May 22, 2025, and at all other distribution centres by May 26, 2025 Further, we will be encountering a supply interruption on our Heparin Sodium Injection, USP 10 000 USP units/mL SD Vial 0.5 mL effective April 30, 2025, until June 2, 2025.
Health Canada comments