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CEFOTAXIME SODIUM FOR INJECTION BP DIN 02352168

Status: Approved
Holder: AUROBINDO PHARMA LIMITED (UNIT VI)
Molecule: CEFOTAXIME SODIUM

Health Canada record

Active ingredient(s)CEFOTAXIME SODIUM 0.5 G
Dosage formPowder For Solution
RouteIntramuscular; Intravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ01DD01 CEFOTAXIME
Original market date
Current status date28-May-2010
SourceHealth Canada DPD

Establishment licence of the holder

Aurobindo Pharma Ltd. (Unit VI) — licence , not currently licensed, last inspection rating C (2024-11-28).

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
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
02225085CLAFORAN - PWS INJ 500MG/VIALSANOFI-AVENTIS CANADA INCPowder For SolutionCEFOTAXIME SODIUM 500 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
114442010-05-28Abbreviated New Drug Submission (ANDS)

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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