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CEFOTAXIME SODIUM FOR INJECTION BP DIN 02352176

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

Health Canada record

Active ingredient(s)CEFOTAXIME SODIUM 1 G
Dosage formPowder For Solution
RouteIntravenous; Intramuscular
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
02352168CEFOTAXIME SODIUM FOR INJECTION BPAUROBINDO PHARMA LIMITED (UNIT VI)Powder For SolutionCEFOTAXIME SODIUM 0.5 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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