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FACTREL DIN 00573760

Status: Marketed
Holder: ZOETIS CANADA INC
Molecule: GONADORELIN (GONADORELIN HYDROCHLORIDE)

Health Canada record

Active ingredient(s)GONADORELIN (GONADORELIN HYDROCHLORIDE) 50 MCG
Dosage formSolution
RouteIntramuscular
SchedulePRESCRIPTION
ClassVeterinary
ATC
Original market date31-Dec-1983
Current status date17-Oct-2016
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 GONADORELIN (GONADORELIN HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02041820FACTREL PWS 500MCG/VIALWYETH-AYERST CANADA INC.Powder For SolutionGONADORELIN (GONADORELIN HYDROCHLORIDE) 500 MCGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
205632018-03-06Supplement to a New Drug Submission (SNDS)CHANGE IN PACKAGING
178612016-03-10Supplement to a New Drug Submission (SNDS)CHANGE IN DOSE, ADDITIONAL MANUFACTURING SITE, MANUFACTURING CHANGES
165352015-01-19Supplement to a New Drug Submission (SNDS)ADDITIONAL CLAIM
153092014-02-24New Drug Submission (NDS)TRANSFER OF DRUG IDENTIFICATION NUMBER (DIN) HOLDER
123822011-06-01Supplement to a New Drug Submission (SNDS)Change to withdrawal period
120062011-01-18New Drug Submission (NDS)Change in DIN ownership
85122007-01-09New Drug Submission (NDS)
67451998-05-15New Drug Submission (NDS)
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