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Version v14-FR Version v8-EN
Language French English
Date Updated 2023-07-04 2022-10-04
Drug Identification Number 02474921 02474921
Brand name PROBUPHINE PROBUPHINE
Common or Proper name Buprenorphine hydrochloride implant Buprenorphine hydrochloride implant
Company Name KNIGHT THERAPEUTICS INC. KNIGHT THERAPEUTICS INC.
Ingredients BUPRENORPHINE HYDROCHLORIDE BUPRENORPHINE HYDROCHLORIDE
Strength(s) 80MG 80MG
Dosage form(s) IMPLANT IMPLANT
Route of administration SUBCUTANEOUS SUBCUTANEOUS SUBCUTANEOUS SUBCUTANEOUS
Packaging size Implant kit has 4 individually pouched Probuphine implants. Implant kit has 4 individually pouched Probuphine implants.
ATC code N07BC N07BC
ATC description
Reason for discontinuation Other (Please describe in comments) Other (Please describe in comments)
Anticipated discontinuation date 2023-05-30 2023-05-30
Actual discontinuation date 2023-07-03
Remaining supply date 2023-05-30 2023-05-30
Discontinuation status Discontinued To be discontinued
Discontinuation decision reversal no no
Tier 3 Status No No
Information on remaining supply
Company comments We regret to announce that following inventory depletion, this product will be officially discontinued and will no longer be marketed in Canada. The reason for discontinuation is due to the inability to successfully acquire continued supply and is unrelated to any safety concerns. We regret to announce that following inventory depletion, this product will be officially discontinued and will no longer be marketed in Canada. The reason for discontinuation is due to the inability to successfully acquire continued supply and is unrelated to any safety concerns.
Health Canada comments