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CEFOXITIN FOR INJECTION DIN 02128187

Status: Marketed
Holder: TEVA CANADA LIMITED
Molecule: CEFOXITIN (CEFOXITIN SODIUM)
Available to quote

Health Canada record

Active ingredient(s)CEFOXITIN (CEFOXITIN SODIUM) 1 G
Dosage formPowder For Solution
RouteIntramuscular; Intravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ01DC01 CEFOXITIN
Original market date31-Dec-1995
Current status date22-Nov-2013
SourceHealth Canada DPD

Establishment licence of the holder

Teva Canada Limited — licence 101810, currently licensed, last inspection rating C (2025-03-04).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing CEFOXITIN (CEFOXITIN SODIUM)

DINProductCompanyFormStrengthStatus
02128195CEFOXITIN FOR INJECTIONTEVA CANADA LIMITEDPowder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 2 GMarketed
02240773CEFOXITIN FOR INJECTIONTEVA CANADA LIMITEDPowder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 10 GCancelled Post Market
02291738CEFOXITIN FOR INJECTION USPPFIZER CANADA ULCPowder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 2 GCancelled Post Market
02291711CEFOXITIN FOR INJECTION USPPFIZER CANADA ULCPowder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 1 GCancelled Post Market
00893668MEFOXIN INJ 1GM/VIAL ADD-VANTAGMERCK FROSST CANADA & CIE, MERCK FROSST CANADA & CO.Powder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 1 GCancelled Post Market
00893676MEFOXIN INJ 2GM/VIAL ADD-VANTAGMERCK FROSST CANADA & CIE, MERCK FROSST CANADA & CO.Powder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 2 GCancelled Post Market
00663697MEFOXIN PWS 1GM/VIALMERCK FROSST CANADA & CIE, MERCK FROSST CANADA & CO.Powder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 1 GCancelled Post Market
00663700MEFOXIN PWS 2GM/VIALMERCK FROSST CANADA & CIE, MERCK FROSST CANADA & CO.Powder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 2 GCancelled Post Market
01980653MEFOXIN PWS INJ 10GM/VIALMERCK FROSST CANADA & CIE, MERCK FROSST CANADA & CO.Powder For SolutionCEFOXITIN (CEFOXITIN SODIUM) 10 GCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
149242013-11-21New Drug Submission (NDS)MANUFACTURER NAME CHANGE
16261999-09-21Supplement to a New Drug Submission (SNDS)PRODUCT NAME CHANGE
58621994-08-17New Drug Submission (NDS)
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