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NEXGARD SPECTRA DIN 02473399

Status: Marketed
Holder: BOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.
Molecule: AFOXOLANER

Health Canada record

Active ingredient(s)AFOXOLANER 75 MG; MILBEMYCIN OXIME 15 MG
Dosage formTablet (Chewable)
RouteOral
SchedulePRESCRIPTION
ClassVeterinary
ATC
Original market date07-Jan-2019
Current status date22-Jul-2019
SourceHealth Canada DPD

Establishment licence of the holder

Boehringer Ingelheim (Canada) Ltd Ltee — licence 100187, currently licensed, last inspection rating C (2025-03-03).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing AFOXOLANER

DINProductCompanyFormStrengthStatus
02427435NEXGARDBOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 11.3 MGMarketed
02427443NEXGARDBOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 28.3 MGMarketed
02427451NEXGARDBOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 68 MGMarketed
02427478NEXGARDBOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 136 MGMarketed
02473364NEXGARD SPECTRABOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 9.4 MG; MILBEMYCIN OXIME 1.9 MGMarketed
02473372NEXGARD SPECTRABOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 18.8 MG; MILBEMYCIN OXIME 3.8 MGMarketed
02473380NEXGARD SPECTRABOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 37.5 MG; MILBEMYCIN OXIME 7.5 MGMarketed
02473402NEXGARD SPECTRABOEHRINGER INGELHEIM ANIMAL HEALTH CANADA INC.Tablet (Chewable)AFOXOLANER 150 MG; MILBEMYCIN OXIME 30 MGMarketed

Notices of Compliance

NOCDateSubmissionReason
257132021-04-22Supplement to a New Drug Submission (SNDS)ADDITIONAL INDICATIONS
236252020-05-19Supplement to a New Drug Submission (SNDS)ALTERNATE DRUG SUBSTANCE MANUFACTURING SITE (MILBEMYCIN OXIME)
233512020-03-17Supplement to a New Drug Submission (SNDS)Additional indication
224202019-07-22New Drug Submission (NDS)Administrative - Manufacturer Name Change
205422018-03-01New Drug Submission (NDS)
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