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GRANISETRON HYDROCHLORIDE INJECTION DIN 02384108

Status: Approved
Holder: STRIDES PHARMA CANADA INC
Molecule: GRANISETRON (GRANISETRON HYDROCHLORIDE)

Health Canada record

Active ingredient(s)GRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MG
Dosage formSolution
RouteIntravenous
SchedulePRESCRIPTION
ClassHuman
ATCA04AA02 GRANISETRON
Original market date
Current status date18-Aug-2020
SourceHealth Canada DPD

Establishment licence of the holder

Strides Pharma Canada Inc. — licence 3-002485, currently licensed, last inspection rating C (2026-03-10).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing GRANISETRON (GRANISETRON HYDROCHLORIDE)

DINProductCompanyFormStrengthStatus
02308894APO-GRANISETRONAPOTEX INCTabletGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGMarketed
02322765GRANISETRON HYDROCHLORIDE INJECTIONOMEGA LABORATORIES LIMITEDLiquidGRANISETRON (GRANISETRON HYDROCHLORIDE) 1 MGMarketed
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
240652020-08-18Abbreviated New Drug Submission (ANDS)Administrative: Change in Product Ownership
157902014-07-09Abbreviated New Drug Submission (ANDS)MERGER - BUYOUT
132162012-04-23Abbreviated New Drug Submission (ANDS)Manufacturer name change
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