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CEFTIOCYL DIN 02417677

Status: Cancelled Post Market
Holder: VETOQUINOL N A INC
Molecule: CEFTIOFUR (CEFTIOFUR HYDROCHLORIDE)

Health Canada record

Active ingredient(s)CEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 50 MG
Dosage formSuspension
RouteIntramuscular; Subcutaneous
SchedulePRESCRIPTION
ClassVeterinary
ATC
Original market date13-May-2014
Current status date02-Jun-2022
SourceHealth Canada DPD

Establishment licence of the holder

Vetoquinol N A Inc. — licence 100448, currently licensed, last inspection rating C (2025-10-20).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing CEFTIOFUR (CEFTIOFUR HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02458861CEVAXEL RTUCEVA ANIMAL HEALTH INCSuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 50 MGMarketed
02443260EFICURLABORATORIOS HIPRA S.A.SuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 50 MGMarketed
02317214EXCENEL RTU EZZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 50 MGMarketed
02312654SPECTRAMAST DCZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 500 MGMarketed
02298325SPECTRAMAST LCZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 125 MGMarketed
02239274EXCENEL RTUZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR HYDROCHLORIDE) 50 MGDormant

Notices of Compliance

NOCDateSubmissionReason
250292021-01-19Supplement to an Abbreviated New Drug Submission (SANDS)MANUFACTURING CHANGES FOR DRUG PRODUCT
149832013-12-04Abbreviated New Drug Submission (ANDS)
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