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ACYCLOVIR SODIUM FOR INJECTION DIN 02231356

Status: Cancelled Post Market
Holder: ABBOTT LABORATORIES, LIMITED
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 date11-Feb-1998
Current status date31-Jul-2007
SourceHealth Canada DPD

Establishment licence of the holder

Abbott Laboratories Co. — licence 3-002635, currently licensed, last inspection rating C (2024-09-23).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ACYCLOVIR (ACYCLOVIR SODIUM)

DINProductCompanyFormStrengthStatus
02236926ACYCLOVIR SODIUM INJECTIONFRESENIUS KABI CANADA LTDSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02531224ACYCLOVIR SODIUM INJECTIONEUGIA PHARMA INC.SolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02494558ACYCLOVIR SODIUM INJECTIONAURO PHARMA INCSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02231190ACYCLOVIR SODIUM FOR INJECTIONNOVOPHARM LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 500 MGCancelled Post Market
02231191ACYCLOVIR SODIUM FOR INJECTIONNOVOPHARM LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market
02231357ACYCLOVIR SODIUM FOR INJECTIONABBOTT LABORATORIES, LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled 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
00605336ZOVIRAXGLAXOSMITHKLINE INCPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 500 MGCancelled Post Market
00899321ZOVIRAXGLAXOSMITHKLINE INCPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
32611997-05-26Abbreviated New Drug Submission (ANDS)
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