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ZOVIRAX DIN 00605336

Status: Cancelled Post Market
Holder: GLAXOSMITHKLINE INC
Molecule: ACYCLOVIR (ACYCLOVIR SODIUM)

Health Canada record

Active ingredient(s)ACYCLOVIR (ACYCLOVIR SODIUM) 500 MG
Dosage formPowder For Solution
RouteIntravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ05AB01 ACYCLOVIR
Original market date31-Dec-1983
Current status date08-Oct-2002
SourceHealth Canada DPD

Establishment licence of the holder

GlaxoSmithKline Inc. — licence 100630, currently licensed, last inspection rating C (2025-09-15).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ACYCLOVIR (ACYCLOVIR SODIUM)

DINProductCompanyFormStrengthStatus
02494558ACYCLOVIR SODIUM INJECTIONAURO PHARMA INCSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02531224ACYCLOVIR SODIUM INJECTIONEUGIA PHARMA INC.SolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02236926ACYCLOVIR SODIUM INJECTIONFRESENIUS KABI CANADA LTDSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02231357ACYCLOVIR SODIUM FOR INJECTIONABBOTT LABORATORIES, LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market
02231356ACYCLOVIR SODIUM FOR INJECTIONABBOTT LABORATORIES, LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 500 MGCancelled Post Market
02231191ACYCLOVIR SODIUM FOR INJECTIONNOVOPHARM LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market
02231190ACYCLOVIR SODIUM FOR INJECTIONNOVOPHARM LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 500 MGCancelled Post Market
02236916ACYCLOVIR SODIUM INJECTIONPFIZER CANADA ULCSolutionACYCLOVIR (ACYCLOVIR SODIUM) 25 MGCancelled Post Market
02239743ACYCLOVIR SODIUM INJECTIONIVAX PHARMACEUTICALS INCORPORATEDSolutionACYCLOVIR (ACYCLOVIR SODIUM) 25 MGCancelled Pre Market
02456524ACYCLOVIR SODIUM INJECTIONSTERIMAX INCSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGDormant
00899321ZOVIRAXGLAXOSMITHKLINE INCPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
8822001-08-07New Drug Submission (NDS)CHANGE IN MANUFACTURER NAME
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