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CAMPTOSAR DIN 02231622

Status: Cancelled Post Market
Holder: PFIZER CANADA ULC
Molecule: IRINOTECAN HYDROCHLORIDE

Health Canada record

Active ingredient(s)IRINOTECAN HYDROCHLORIDE 20 MG
Dosage formSolution
RouteIntravenous
SchedulePRESCRIPTION
ClassHuman
ATCL01CE02 IRINOTECAN
Original market date27-Aug-1997
Current status date02-Jun-2022
SourceHealth Canada DPD

Establishment licence of the holder

Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing IRINOTECAN HYDROCHLORIDE

DINProductCompanyFormStrengthStatus
02312409IRINOTECAN FOR INJECTIONTEVA CANADA LIMITEDSolutionIRINOTECAN HYDROCHLORIDE 20 MGMarketed
02528800IRINOTECAN HYDROCHLORIDE INJECTIONEUGIA PHARMA INC.SolutionIRINOTECAN HYDROCHLORIDE 100 MGMarketed
02528770IRINOTECAN HYDROCHLORIDE INJECTIONEUGIA PHARMA INC.SolutionIRINOTECAN HYDROCHLORIDE 40 MGApproved
02528789IRINOTECAN HYDROCHLORIDE INJECTIONEUGIA PHARMA INC.SolutionIRINOTECAN HYDROCHLORIDE 500 MGMarketed
02528797IRINOTECAN HYDROCHLORIDE INJECTIONEUGIA PHARMA INC.SolutionIRINOTECAN HYDROCHLORIDE 300 MGApproved
02501260IRINOTECAN HYDROCHLORIDE INJECTIONAURO PHARMA INCSolutionIRINOTECAN HYDROCHLORIDE 40 MGApproved
02501279IRINOTECAN HYDROCHLORIDE INJECTIONAURO PHARMA INCSolutionIRINOTECAN HYDROCHLORIDE 100 MGMarketed
02501287IRINOTECAN HYDROCHLORIDE INJECTIONAURO PHARMA INCSolutionIRINOTECAN HYDROCHLORIDE 300 MGApproved
02501295IRINOTECAN HYDROCHLORIDE INJECTIONAURO PHARMA INCSolutionIRINOTECAN HYDROCHLORIDE 500 MGMarketed
02258218IRINOTECAN HYDROCHLORIDE INJECTION USPPFIZER CANADA ULCSolutionIRINOTECAN HYDROCHLORIDE 20 MGMarketed
02410419IRINOTECANPFIZER CANADA ULCSolutionIRINOTECAN HYDROCHLORIDE 20 MGCancelled Post Market
02305143IRINOTECAN HYDROCHLORIDE TRIHYDRATE INJECTIONSANDOZ CANADA INCORPORATEDSolutionIRINOTECAN HYDROCHLORIDE 20 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
13952003-09-11New Drug Submission (NDS)MANUFACTURER NAME CHANGE
23462001-02-13New Drug Submission (NDS)MANUFACTURER NAME CHANGE
38841997-07-04New Drug Submission (NDS)

International API supply for IRINOTECAN HYDROCHLORIDE

15 active FDA Drug Master Files.

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