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WINRHO SDF DIN 02302578

Status: Marketed
Holder: KI BIOPHARMA LLC
Molecule: ANTI-D (RH) IMMUNOGLOBULIN (HUMAN)

Health Canada record

Active ingredient(s)ANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 1500 UNIT
Dosage formSolution
RouteIntravenous; Intramuscular
ScheduleSCHEDULE D
ClassHuman
ATCJ06BB01 ANTI-D (RH) IMMUNOGLOBULIN
Original market date16-Jun-2008
Current status date11-Jul-2022
SourceHealth Canada DPD

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
02562405HYPERRHOGRIFOLS THERAPEUTICS LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 250 UNITApproved
02302551WINRHO SDFKI BIOPHARMA LLCSolutionANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 600 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
02230397WINRHO SDFAPTEVO BIOTHERAPEUTICS LLCKitANTI-D (RH) IMMUNOGLOBULIN (HUMAN) 5000 UNITCancelled 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

Notices of Compliance

NOCDateSubmissionReason
284712022-06-27New Drug Submission (NDS)Administrative ¿ Change in Product Ownership
202832018-01-11New Drug Submission (NDS)TRANSFER OF DRUG IDENTIFICATION NUMBER (DIN)
91942007-11-23Supplement to a New Drug Submission (SNDS)NEW LIQUID FORMULATION
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