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AMIKACIN SULFATE INJECTION USP DIN 02242971

Status: Marketed
Holder: SANDOZ CANADA INCORPORATED
Molecule: AMIKACIN (AMIKACIN SULFATE)
Available to quote

Health Canada record

Active ingredient(s)AMIKACIN (AMIKACIN SULFATE) 250 MG
Dosage formLiquid
RouteIntramuscular; Intravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ01GB06 AMIKACIN
Original market date29-Jan-2001
Current status date16-Sep-2005
SourceHealth Canada DPD

Establishment licence of the holder

Sandoz Canada Incorporated — licence 101370, currently licensed, last inspection rating C (2025-02-25).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing AMIKACIN (AMIKACIN SULFATE)

DINProductCompanyFormStrengthStatus
02173336AMIGLYDE-VZOETIS CANADA INCSolutionAMIKACIN (AMIKACIN SULFATE) 250 MGMarketed
02486717AMIKACIN SULFATE INJECTIONOMEGA LABORATORIES LIMITEDSolutionAMIKACIN (AMIKACIN SULFATE) 250 MGMarketed
02529459AMIKACIN SULFATE INJECTIONJAMP PHARMA CORPORATIONSolutionAMIKACIN (AMIKACIN SULFATE) 250 MGMarketed
02481073AMIKACIN SULFATE INJECTION USPMARCAN PHARMACEUTICALS INCSolutionAMIKACIN (AMIKACIN SULFATE) 500 MGMarketed
02525909AMIKACIN SULFATE INJECTIONHIKMA CANADA LIMITEDSolutionAMIKACIN (AMIKACIN SULFATE) 250 MGCancelled Post Market
02539535AMIKACIN SULFATE INJECTIONJUNO PHARMACEUTICALS CORP.SolutionAMIKACIN (AMIKACIN SULFATE) 250 MGCancelled Pre Market
00397415AMIKINBRISTOL-MYERS SQUIBB CANADASolutionAMIKACIN (AMIKACIN SULFATE) 250 MGCancelled Post Market
02489147ERFA-AMIKACINSEARCHLIGHT PHARMA INCSolutionAMIKACIN (AMIKACIN SULFATE) 250 MGCancelled Post Market
02506599VPI-AMIKACINVPI PHARMACEUTICALS INCSolutionAMIKACIN (AMIKACIN SULFATE) 500 MGDormant

Notices of Compliance

NOCDateSubmissionReason
73782005-09-15Abbreviated New Drug Submission (ANDS)MANUFACTURER NAME CHANGE
9392000-11-28Abbreviated New Drug Submission (ANDS)
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