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RECOMBIVAX HB (WITH PRESERVATIVE) DIN 00749486

Status: Cancelled Post Market
Holder: MERCK CANADA INC
Molecule: HEPATITIS B SURFACE ANTIGEN (RECOMBINANT)

Health Canada record

Active ingredient(s)HEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCG
Dosage formSolution
RouteIntramuscular
ScheduleSCHEDULE D
ClassHuman
ATCJ07BC01 HEPATITIS B, PURIFIED ANTIGEN
Original market date31-Dec-1987
Current status date08-Mar-2010
SourceHealth Canada DPD

Establishment licence of the holder

Merck Canada Inc — licence 101380, currently licensed, last inspection rating C (2023-07-17).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing HEPATITIS B SURFACE ANTIGEN (RECOMBINANT)

DINProductCompanyFormStrengthStatus
02487039ENGERIX-BGLAXOSMITHKLINE INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 20 MCGMarketed
02487020ENGERIX-BGLAXOSMITHKLINE INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCGMarketed
02533286PREHEVBRIOVBI VACCINES INC.SuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCGApproved
02561476RECOMBIVAX HBMERCK CANADA INCSolutionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 5 MCGMarketed
02245977RECOMBIVAX HBMERCK CANADA INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 40 MCGMarketed
02561484RECOMBIVAX HBMERCK CANADA INCSolutionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCGMarketed
02237548TWINRIX JUNIORGLAXOSMITHKLINE INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCG; HEPATITIS A VIRUS, INACTIVATED 360 UNITMarketed
02296454ENGERIX-BGLAXOSMITHKLINE INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCGCancelled Post Market
01919431ENGERIX-BGLAXOSMITHKLINE INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 20 MCGCancelled Post Market
02243676RECOMBIVAX HBMERCK CANADA INCSuspensionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 10 MCGCancelled Post Market
01934023RECOMBIVAX HB (ADULT DIALYSIS WITH PRESERVATIVE)MERCK CANADA INCSolutionHEPATITIS B SURFACE ANTIGEN (RECOMBINANT) 40 MCGCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
73832005-09-16New Drug Submission (NDS)MANUFACTURER NAME CHANGE
12102000-06-12New Drug Submission (NDS)
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