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ACYCLOVIR SODIUM INJECTION DIN 02236916

Status: Cancelled Post Market
Holder: PFIZER CANADA ULC
Molecule: ACYCLOVIR (ACYCLOVIR SODIUM)

Health Canada record

Active ingredient(s)ACYCLOVIR (ACYCLOVIR SODIUM) 25 MG
Dosage formSolution
RouteIntravenous
SchedulePRESCRIPTION
ClassHuman
ATCJ05AB01 ACYCLOVIR
Original market date18-Mar-1998
Current status date09-May-2024
SourceHealth Canada DPD

Establishment licence of the holder

Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ACYCLOVIR (ACYCLOVIR SODIUM)

DINProductCompanyFormStrengthStatus
02531224ACYCLOVIR SODIUM INJECTIONEUGIA PHARMA INC.SolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02494558ACYCLOVIR SODIUM INJECTIONAURO PHARMA INCSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02236926ACYCLOVIR SODIUM INJECTIONFRESENIUS KABI CANADA LTDSolutionACYCLOVIR (ACYCLOVIR SODIUM) 50 MGMarketed
02231356ACYCLOVIR SODIUM FOR INJECTIONABBOTT LABORATORIES, LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 500 MGCancelled Post Market
02231357ACYCLOVIR SODIUM FOR INJECTIONABBOTT LABORATORIES, LIMITEDPowder For SolutionACYCLOVIR (ACYCLOVIR SODIUM) 1 GCancelled Post Market
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
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
196482017-08-10Abbreviated New Drug Submission (ANDS)MERGER - BUYOUT
183402016-08-05Supplement to an Abbreviated New Drug Submission (SANDS)REIVISIONS TO THE LABELS, PACKAGE INSERTN AND PRESCRIBING INFORMATION
88202007-06-07Abbreviated New Drug Submission (ANDS)MANUFACTURER NAME CHANGE
1952002-11-01Abbreviated New Drug Submission (ANDS)MANUFACTURER NAME CHANGE
26971998-03-04Abbreviated New Drug Submission (ANDS)
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