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PANACUR PASTE 10% DIN 02113163

Status: Marketed
Holder: INTERVET CANADA CORP
Molecule: FENBENDAZOLE

Health Canada record

Active ingredient(s)FENBENDAZOLE 100 MG
Dosage formPaste
RouteOral
ScheduleNON-PRESCRIPTION DRUGS
ClassVeterinary
ATC
Original market date31-Dec-1989
Current status date16-Oct-2001
SourceHealth Canada DPD

Establishment licence of the holder

Intervet Canada Corp. — licence 100147, currently licensed, last inspection rating C (2023-07-17).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing FENBENDAZOLE

DINProductCompanyFormStrengthStatus
02458535PANACUR AQUASOLINTERVET CANADA CORPSuspensionFENBENDAZOLE 200 MGMarketed
02297043PANACUR GRANULE SINGLESINTERVET CANADA CORPPowderFENBENDAZOLE 222 MGMarketed
00489883PANACUR GRANULES 22.2%INTERVET CANADA CORPPowderFENBENDAZOLE 222 MGMarketed
00489875PANACUR SUSPENSION 10%INTERVET CANADA CORPSuspensionFENBENDAZOLE 100 MGMarketed
02069490SAFE-GUARD PASTE 10%INTERVET CANADA CORPPasteFENBENDAZOLE 100 MGMarketed
00617598SAFE-GUARD PREMIX 20%INTERVET CANADA CORPDrug PremixFENBENDAZOLE 200 MGMarketed
02113171SAFE-GUARD SUSPENSION 10%INTERVET CANADA CORPSuspensionFENBENDAZOLE 10 %Marketed
02240614NOROFEN WORMERNORBROOK LABORATORIES LTD.GranulesFENBENDAZOLE 220 MGCancelled Pre Market
00896543PREMELANGE 25/2 PORCS MEDICAMENTE 8GM/KGLA COOP FEDEREEDrug PremixFENBENDAZOLE 8 GCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
62462001-03-27Supplement to a New Drug Submission (SNDS)TREATMENT OF EQUINE LARVAL CYATHOSTOMOSIS INDUCED BY ENCYSTED LARVAE (THIRD AND FOURTH STAGE) OF CYATHOSTOMES
64912000-08-30New Drug Submission (NDS)
64922000-08-30Supplement to a New Drug Submission (SNDS)CHANGE IN EXPIRATION DATE TO 42 MONTHS (25GM PACKAGE), 36 MONTHS (290GM PACKAGE); CHANGE IN MANUFACTURING SITE

International API supply for FENBENDAZOLE

0 active FDA Drug Master Files.

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