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Version v2-FR Version v2-FR
Language French French
Date Updated 2024-12-24 2024-12-24
Drug Identification Number 02046210 02046210
Brand name LUTREPULSE PWS 0.8MG/VIAL LUTREPULSE PWS 0.8MG/VIAL
Common or Proper name Gonadorelin Acetate Gonadorelin Acetate
Company Name FERRING INC FERRING INC
Ingredients GONADORELIN ACETATE GONADORELIN ACETATE
Strength(s) 0.8MG 0.8MG
Dosage form(s) POWDER FOR SOLUTION POWDER FOR 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 10mL vial 10mL vial
ATC code H01CA H01CA
ATC description HYPOTHALAMIC HORMONES HYPOTHALAMIC HORMONES
Reason for discontinuation Manufacturing issues Manufacturing issues
Anticipated discontinuation date
Actual discontinuation date 2024-11-26 2024-11-26
Remaining supply date
Discontinuation status Discontinued Discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments Lutrapulse 0.8mg is no longer available worldwide beyond June 30, 2024 due to expiry dating of existing supply. No new product will be manufactured or is available due to manufacturing line decommissioning. Lutrapulse 0.8mg is no longer available worldwide beyond June 30, 2024 due to expiry dating of existing supply. No new product will be manufactured or is available due to manufacturing line decommissioning.
Health Canada comments