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EXCEDE 200 DIN 02360586

Status: Marketed
Holder: ZOETIS CANADA INC
Molecule: CEFTIOFUR (CEFTIOFUR CRYSTALLINE FREE ACID)

Health Canada record

Active ingredient(s)CEFTIOFUR (CEFTIOFUR CRYSTALLINE FREE ACID) 200 MG
Dosage formSuspension
RouteIntramuscular; Subcutaneous
SchedulePRESCRIPTION
ClassVeterinary
ATC
Original market date22-Nov-2011
Current status date02-Sep-2014
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 CRYSTALLINE FREE ACID)

DINProductCompanyFormStrengthStatus
02305453EXCEDE 100ZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR CRYSTALLINE FREE ACID) 100 MGMarketed
02292149EXCEDEZOETIS CANADA INCSuspensionCEFTIOFUR (CEFTIOFUR CRYSTALLINE FREE ACID) 200 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
150912014-01-02New Drug Submission (NDS)TRANSFER OF DRUG IDENTIFICATION (DIN) HOLDER
136792012-09-28Supplement to a New Drug Submission (SNDS)Change in withholding time
132702012-05-03Supplement to a New Drug Submission (SNDS)New indications
119392010-12-20New Drug Submission (NDS)
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