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APO-GRANISETRON DIN 02308894

Status: Marketed
Holder: APOTEX INC
Molecule: GRANISETRON (GRANISETRON HYDROCHLORIDE)
Available to quote

Health Canada record

Active ingredient(s)GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCA04AA02 GRANISETRON
Original market date20-Feb-2009
Current status date16-Sep-2016
SourceHealth Canada DPD

Establishment licence of the holder

Apotex Inc — licence 100375, currently licensed, last inspection rating C (2026-04-21).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing GRANISETRON (GRANISETRON HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02322765GRANISETRON HYDROCHLORIDE INJECTIONOMEGA LABORATORIES LIMITEDLiquidGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGMarketed
02384108GRANISETRON HYDROCHLORIDE INJECTIONSTRIDES PHARMA CANADA INCSolutionGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGApproved
02558408GRANISETRON HYDROCHLORIDE INJECTION USPHIKMA CANADA LIMITEDSolutionGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGApproved
02452359NAT-GRANISETRONNATCO PHARMA (CANADA) INCTabletGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGMarketed
02304708GRANISETRON HYDROCHLORIDE INJECTIONSANDOZ CANADA INCORPORATEDLiquidGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGCancelled Post Market
02385414GRANISETRON HYDROCHLORIDE INJECTION SDZSANDOZ CANADA INCORPORATEDSolutionGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGCancelled Post Market
02472686JAMP GRANISETRONJAMP PHARMA CORPORATIONTabletGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGDormant
02088371KYTRIL 1MG/1MLHOFFMANN-LA ROCHE LIMITEDLiquidGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGCancelled Post Market
02185881KYTRIL TABLETS 1MGHOFFMANN-LA ROCHE LIMITEDTabletGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
182432016-07-08Abbreviated New Drug Submission (ANDS)Updates to the Labels Administrative - Transfer of Drug Identification Number
116182010-07-26Abbreviated New Drug Submission (ANDS)Manufacturer and product name change
100422009-02-19Abbreviated New Drug Submission (ANDS)
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