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ZYVOXAM 600 MG DIN 02243684

Status: Cancelled Post Market
Holder: PFIZER CANADA ULC
Molecule: LINEZOLID

Health Canada record

Active ingredient(s)LINEZOLID 600 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCJ01XX08 LINEZOLID
Original market date06-Apr-2001
Current status date31-Jul-2020
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 LINEZOLID

DINProductCompanyFormStrengthStatus
02426552APO-LINEZOLIDAPOTEX INCTabletLINEZOLID 600 MGMarketed
02520354JAMP LINEZOLIDJAMP PHARMA CORPORATIONTabletLINEZOLID 600 MGMarketed
02539748LINEZOLID INJECTIONEUGIA PHARMA INC.SolutionLINEZOLID 2 MGMarketed
02469294LINEZOLID INJECTIONAURO PHARMA INCSolutionLINEZOLID 2 MGApproved
02461897LINEZOLID INJECTIONPHARMARIS CANADA INCSolutionLINEZOLID 2 MGApproved
02430827LINEZOLID INJECTIONFRESENIUS KABI CANADA LTDSolutionLINEZOLID 2 MGMarketed
02481278LINEZOLID INJECTIONJAMP PHARMA CORPORATIONSolutionLINEZOLID 2 MGMarketed
02486156LINEZOLID TABLETSSTRIDES PHARMA CANADA INCTabletLINEZOLID 600 MGApproved
02422689SANDOZ LINEZOLIDSANDOZ CANADA INCORPORATEDTabletLINEZOLID 600 MGMarketed
02243685ZYVOXAMPFIZER CANADA ULCSolutionLINEZOLID 2 MGMarketed
02243686ZYVOXAMPFIZER CANADA ULCPowder For SuspensionLINEZOLID 100 MGMarketed
02457903LINEZOLIDPANDA PHARMACEUTICALS INC.TabletLINEZOLID 600 MGCancelled Pre Market
02441012LINEZOLID INJECTIONHOSPIRA HEALTHCARE ULCSolutionLINEZOLID 2 MGCancelled Pre Market
02429527LINEZOLID INJECTIONSANDOZ CANADA INCORPORATEDSolutionLINEZOLID 2 MGCancelled Pre Market
02402637LINEZOLID INJECTIONTEVA CANADA LIMITEDSolutionLINEZOLID 2 MGCancelled Post Market
02462214LINEZOLID INJECTIONMDA INC.SolutionLINEZOLID 2 MGCancelled Pre Market
02470551LINEZOLID INTRAVENOUS INJECTIONMDA INC.SolutionLINEZOLID 600 MGCancelled Pre Market
02359235NOVO-LINEZOLIDTEVA CANADA LIMITEDTabletLINEZOLID 600 MGCancelled Pre Market

Notices of Compliance

NOCDateSubmissionReason
15672003-09-15New Drug Submission (NDS)MANUFACTURER NAME CHANGE
23792001-04-02New Drug Submission (NDS)

International API supply for LINEZOLID

31 active FDA Drug Master Files.

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