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JAKAVI DIN 02388022

Status: Marketed
Holder: NOVARTIS PHARMACEUTICALS CANADA INC
Molecule: RUXOLITINIB (RUXOLITINIB PHOSPHATE)
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Health Canada record

Active ingredient(s)RUXOLITINIB (RUXOLITINIB PHOSPHATE) 20 MG
Dosage formTablet
RouteOral
SchedulePRESCRIPTION
ClassHuman
ATCL01EJ01 RUXOLITINIB
Original market date19-Jul-2012
Current status date19-Jul-2012
SourceHealth Canada DPD

Establishment licence of the holder

Novartis Pharmaceuticals Canada Inc — licence 100273, currently licensed, last inspection rating C (2025-01-14).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing RUXOLITINIB (RUXOLITINIB PHOSPHATE)

DINProductCompanyFormStrengthStatus
02388006JAKAVINOVARTIS PHARMACEUTICALS CANADA INCTabletRUXOLITINIB (RUXOLITINIB PHOSPHATE) 5 MGMarketed
02388014JAKAVINOVARTIS PHARMACEUTICALS CANADA INCTabletRUXOLITINIB (RUXOLITINIB PHOSPHATE) 15 MGMarketed
02434814JAKAVINOVARTIS PHARMACEUTICALS CANADA INCTabletRUXOLITINIB (RUXOLITINIB PHOSPHATE) 10 MGMarketed
02552434OPZELURAINCYTE CORPORATIONCreamRUXOLITINIB (RUXOLITINIB PHOSPHATE) 1.5 %Marketed

Notices of Compliance

NOCDateSubmissionReason
134042012-06-19New Drug Submission (NDS)
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