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EXCENEL DIN 00813567

Status: Marketed
Holder: ZOETIS CANADA INC
Molecule: CEFTIOFUR (CEFTIOFUR SODIUM)

Health Canada record

Active ingredient(s)CEFTIOFUR (CEFTIOFUR SODIUM) 50 MG
Dosage formPowder For Solution
RouteSubcutaneous; Intramuscular
SchedulePRESCRIPTION
ClassVeterinary
ATC
Original market date31-Dec-1989
Current status date31-Mar-2015
SourceHealth Canada DPD

Establishment licence of the holder

Zoetis Canada Inc — licence 102076, currently licensed, last inspection rating C (2023-10-05).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing CEFTIOFUR (CEFTIOFUR SODIUM)

DINProductCompanyFormStrengthStatus
02412284CEFTIOFUR SODIUM FOR INJECTIONBIO AGRI MIX LPPowder For SolutionCEFTIOFUR (CEFTIOFUR SODIUM) 50 MGMarketed

Notices of Compliance

NOCDateSubmissionReason
150882014-01-02New Drug Submission (NDS)TRANSFER OF DRUG IDENTIFICATION (DIN) HOLDER
139202012-11-30Supplement to a New Drug Submission (SNDS)Removal of species; turkey poults
84852006-12-21New Drug Submission (NDS)
60892002-06-03Supplement to a New Drug Submission (SNDS)ALTERNATE SOURCE OF THE ACTIVE INGREDIENT
61392002-01-21New Drug Submission (NDS)
67431998-07-16Supplement to a New Drug Submission (SNDS)CHANGE IN STORAGE CONDITION
67421998-02-18Supplement to a New Drug Submission (SNDS)ADDITIONAL CLAIM FOR USE IN LAMBS, FOR THE TREATMENT OF RESPIRATORY DISEASE 9PNEUMONIA) ASSOCIATED WITH PASTEURELLA HAEMOLYTICA
66821997-05-15New Drug Submission (NDS)
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