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CLAFORAN - PWS INJ 500MG/VIAL DIN 02225085

Status: Cancelled Post Market
Holder: SANOFI-AVENTIS CANADA INC
Molecule: CEFOTAXIME SODIUM

Health Canada record

Active ingredient(s)CEFOTAXIME SODIUM 500 MG
Dosage formPowder For Solution
RouteIntramuscular; Intravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ01DD01 CEFOTAXIME
Original market date19-Dec-2003
Current status date31-Dec-2012
SourceHealth Canada DPD

Establishment licence of the holder

sanofi-aventis Canada Inc. — licence 101470, currently licensed, last inspection rating C (2026-02-17).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing CEFOTAXIME SODIUM

DINProductCompanyFormStrengthStatus
02352176CEFOTAXIME SODIUM FOR INJECTION BPAUROBINDO PHARMA LIMITED (UNIT VI)Powder For SolutionCEFOTAXIME SODIUM 1 GApproved
02352184CEFOTAXIME SODIUM FOR INJECTION BPAUROBINDO PHARMA LIMITED (UNIT VI)Powder For SolutionCEFOTAXIME SODIUM 2 GApproved
02352168CEFOTAXIME SODIUM FOR INJECTION BPAUROBINDO PHARMA LIMITED (UNIT VI)Powder For SolutionCEFOTAXIME SODIUM 0.5 GApproved
02434105CEFOTAXIME SODIUM FOR INJECTION, BPSTERIMAX INCPowder For SolutionCEFOTAXIME SODIUM 2 GMarketed
02434083CEFOTAXIME SODIUM FOR INJECTION, BPSTERIMAX INCPowder For SolutionCEFOTAXIME SODIUM 500 MGApproved
02434091CEFOTAXIME SODIUM FOR INJECTION, BPSTERIMAX INCPowder For SolutionCEFOTAXIME SODIUM 1 GMarketed
02225093CLAFORAN - PWS INJ 1.0G/VIALSANOFI-AVENTIS CANADA INCPowder For SolutionCEFOTAXIME SODIUM 1 GCancelled Post Market
02225107CLAFORAN - PWS INJ 2.0G/VIALSANOFI-AVENTIS CANADA INCPowder For SolutionCEFOTAXIME SODIUM 2 GCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
78382006-03-21New Drug Submission (NDS)MANUFACTURER NAME CHANGE
10482000-06-12New Drug Submission (NDS)
43001996-07-17New Drug Submission (NDS)

International API supply for CEFOTAXIME SODIUM

0 valid EDQM Certificates of Suitability from 0 holders. 5 active FDA Drug Master Files.

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