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HERZUMA DIN 02506211

Status: Marketed
Holder: CELLTRION INC.
Molecule: TRASTUZUMAB

Health Canada record

Active ingredient(s)TRASTUZUMAB 150 MG
Dosage formPowder For Solution
RouteIntravenous
ScheduleSCHEDULE D; PRESCRIPTION
ClassHuman
ATCL01FD01 TRASTUZUMAB
Original market date25-Feb-2021
Current status date03-Oct-2024
SourceHealth Canada DPD

Establishment licence of the holder

Celltrion Healthcare Canada Limited — licence 3-002622, currently licensed, last inspection rating C (2025-11-12).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing TRASTUZUMAB

DINProductCompanyFormStrengthStatus
02550989ADHEROZAACCORD HEALTHCARE INCPowder For Solution; KitTRASTUZUMAB 420 MGApproved
02550970ADHEROZAACCORD HEALTHCARE INCPowder For SolutionTRASTUZUMAB 150 MGApproved
02240692HERCEPTINHOFFMANN-LA ROCHE LIMITEDPowder For SolutionTRASTUZUMAB 440 MGMarketed
02480697HERCEPTIN SCHOFFMANN-LA ROCHE LIMITEDSolutionTRASTUZUMAB 600 MGMarketed
02480794HERZUMACELLTRION INC.Powder For Solution; KitTRASTUZUMAB 440 MGMarketed
02496690KANJINTIAMGEN CANADA INCKit; Powder For SolutionTRASTUZUMAB 420 MGMarketed
02518244KANJINTIAMGEN CANADA INCPowder For SolutionTRASTUZUMAB 150 MGMarketed
02474425OGIVRIBIOSIMILAR COLLABORATIONS IRELAND LIMITEDPowder For SolutionTRASTUZUMAB 150 MGMarketed
02474433OGIVRIBIOSIMILAR COLLABORATIONS IRELAND LIMITEDPowder For SolutionTRASTUZUMAB 440 MG; WATER 20 MLMarketed
02524325ONTRUZANTSAMSUNG BIOEPIS CO., LTDPowder For SolutionTRASTUZUMAB 440 MGMarketed
02524317ONTRUZANTSAMSUNG BIOEPIS CO., LTDPowder For SolutionTRASTUZUMAB 150 MGMarketed
02512920PHESGOHOFFMANN-LA ROCHE LIMITEDSolutionTRASTUZUMAB 60 MG; PERTUZUMAB 60 MGMarketed
02512912PHESGOHOFFMANN-LA ROCHE LIMITEDSolutionTRASTUZUMAB 40 MG; PERTUZUMAB 80 MGMarketed
02483475TRAZIMERAPFIZER CANADA ULCPowder For SolutionTRASTUZUMAB 150 MGMarketed
02483467TRAZIMERAPFIZER CANADA ULCPowder For SolutionTRASTUZUMAB 440 MGMarketed

Notices of Compliance

NOCDateSubmissionReason
341442024-10-03New Drug Submission (NDS)Administrative ¿ merger/buyout
244782020-10-20Supplement to a New Drug Submission (SNDS)NEW STRENGTH
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