Drug Report History #106800

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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.

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Version v8-FR Version v2-FR
Language French French
Date Updated (Changed) Updated to: 2021-01-18 Was: 2020-02-20
Drug Identification Number 00745626 00745626
Brand name HUMATROPE HUMATROPE
Common or Proper name Somatropin for injection Somatropin for injection
Company Name ELI LILLY CANADA INC ELI LILLY CANADA INC
Ingredients SOMATROPIN SOMATROPIN
Strength(s) 1MG 1MG
Dosage form(s) POWDER FOR SOLUTION POWDER FOR SOLUTION
Route of administration INTRAMUSCULAR SUBCUTANEOUS INTRAMUSCULAR SUBCUTANEOUS
Packaging size (Changed) Updated to: 5 mg vial Was: 5 mg/vial
Additional packaging sizes
ATC code H01AC H01AC
ATC description ANTERIOR PITUITARY LOBE HORMONES AND ANALOGUES ANTERIOR PITUITARY LOBE HORMONES AND ANALOGUES
Reason for discontinuation Business reasons Business reasons
Anticipated discontinuation date (Changed) Updated to: 2021-01-15 Was: 2020-11-01
Actual discontinuation date (Changed) Updated to: 2021-01-15 Was:
Remaining supply date (Changed) Updated to: 2021-01-15 Was: 2020-11-01
Discontinuation status (Changed) Updated to: Discontinued Was: To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments Please contact Eli Lilly Canada's Response Centre 1-888-545-5972 should you have any questions. Please contact Eli Lilly Canada's Response Centre 1-888-545-5972 should you have any questions.
Health Canada comments