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KETOTIFEN OPHTHALMIC SOLUTION DIN 02400871

Status: Dormant
Holder: STERIMAX INC
Molecule: KETOTIFEN (KETOTIFEN FUMARATE)

Health Canada record

Active ingredient(s)KETOTIFEN (KETOTIFEN FUMARATE) 0.25 MG
Dosage formSolution
RouteOphthalmic
SchedulePRESCRIPTION
ClassHuman
ATCS01GX08 KETOTIFEN
Original market date07-Mar-2013
Current status date19-Aug-2021
SourceHealth Canada DPD

Establishment licence of the holder

Sterimax Inc — licence 100925, currently licensed, last inspection rating C (2024-05-13).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing KETOTIFEN (KETOTIFEN FUMARATE)

DINProductCompanyFormStrengthStatus
02542722JAMP KETOTIFEN OPHTHALMICJAMP PHARMA CORPORATIONSolutionKETOTIFEN (KETOTIFEN FUMARATE) 0.25 MGMarketed
00577308ZADITENTEVA CANADA LIMITEDTabletKETOTIFEN (KETOTIFEN FUMARATE) 1 MGMarketed
02172585ZADITEN - DPS 1MG/MLNOVARTIS PHARMACEUTICALS CANADA INCDropsKETOTIFEN (KETOTIFEN FUMARATE) 1 MGApproved
02242324ZADITORLABORATOIRES THEASolutionKETOTIFEN (KETOTIFEN FUMARATE) 0.25 MGMarketed
02176084NOVO-KETOTIFEN - SYR 1MG/5MLNOVOPHARM LIMITEDSyrupKETOTIFEN (KETOTIFEN FUMARATE) 1 MGCancelled Post Market
02230730NOVO-KETOTIFEN TAB 1MGNOVOPHARM LIMITEDTabletKETOTIFEN (KETOTIFEN FUMARATE) 1 MGCancelled Post Market
02231680PMS-KETOTIFENPHARMASCIENCE INCTabletKETOTIFEN (KETOTIFEN FUMARATE) 1 MGCancelled Post Market
02231679PMS-KETOTIFENPHARMASCIENCE INCSyrupKETOTIFEN (KETOTIFEN FUMARATE) 1 MGCancelled Post Market
00600784ZADITENTEVA CANADA LIMITEDSyrupKETOTIFEN (KETOTIFEN FUMARATE) 1 MGCancelled Post Market
02279223ZADITORNOVARTIS PHARMACEUTICALS CANADA INCSolutionKETOTIFEN (KETOTIFEN FUMARATE) 0.25 MGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
140492013-01-30Abbreviated New Drug Submission (ANDS)
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