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HYPERRHO DIN 02562405

Status: Approved
Holder: GRIFOLS THERAPEUTICS LLC
Molecule: ANTI-D (RH) IMMUNOGLOBULIN (HUMAN)

Health Canada record

Active ingredient(s)ANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 250 UNIT
Dosage formSolution
RouteIntramuscular
ScheduleSCHEDULE D
ClassHuman
ATCJ06BA01 IMMUNOGLOBULINS, NORMAL HUMAN, FOR EXTRAVASC. ADM
Original market date
Current status date27-Oct-2025
SourceHealth Canada DPD

Establishment licence of the holder

Grifols Therapeutics LLC — licence , not currently licensed, last inspection rating C (2023-06-03).

No Canadian shortage report is currently matched to this DIN.

Other Canadian products containing ANTI-D (RH) IMMUNOGLOBULIN (HUMAN)

DINProductCompanyFormStrengthStatus
02379457HYPERRHOGRIFOLS THERAPEUTICS LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 1500 UNITApproved
02302551WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 600 UNITMarketed
02302578WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 1500 UNITMarketed
02302586WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 2500 UNITApproved
02302608WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 15000 UNITApproved
02243524HYPERRHO S/D FULL DOSEGRIFOLS THERAPEUTICS LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 1500 UNITCancelled Pre Market
02022842WINRHO SD KIT INJRH PHARMACEUTICALS INC.KitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 120 MCG; SODIUM CHLORIDE 0.9 %Cancelled Post Market
02022834WINRHO SD KIT INJ.RH PHARMACEUTICALS INC.KitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 300 MCG; SODIUM CHLORIDE .9 %Cancelled Post Market
02302594WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 5000 UNITDormant
02217430WINRHO SDFAPTEVO BIOTHERAPEUTICS LLCKitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 600 UNITCancelled Post Market
02217449WINRHO SDFAPTEVO BIOTHERAPEUTICS LLCKitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 1500 UNITCancelled Post Market
02230397WINRHO SDFAPTEVO BIOTHERAPEUTICS LLCKitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 5000 UNITCancelled Post Market

Notices of Compliance

NOCDateSubmissionReason
362632025-10-27Supplement to a New Drug Submission (SNDS)Revised brand name. Alternate drug substance manufacturing facility. Drug substance manufacturing process change. New strength
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