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    NDC 50090-1377-00 BOOSTRIX 8; 2.5; 8; 5; 2.5 ug/.5mL; ug/.5mL; ug/.5mL; [iU]/.5mL; [iU]/.5mL Details

    BOOSTRIX 8; 2.5; 8; 5; 2.5 ug/.5mL; ug/.5mL; ug/.5mL; [iU]/.5mL; [iU]/.5mL

    BOOSTRIX is a INTRAMUSCULAR SUSPENSION in the VACCINE category. It is labeled and distributed by A-S Medication Solutions. The primary component is BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); BORDETELLA PERTUSSIS PERTACTIN ANTIGEN (FORMALDEHYDE INACTIVATED); BORDETELLA PERTUSSIS TOXOID ANTIGEN (FORMALDEHYDE, GLUTARALDEHYDE INACTIVATED); CLOSTRIDIUM TETANI TOXOID.

    Product Information

    NDC 50090-1377
    Product ID 50090-1377_56362763-26c8-4a4e-b9e1-bbb3524d692c
    Associated GPIs 1899000322E620
    GCN Sequence Number 059080
    GCN Sequence Number Description diphth,pertuss(acell),tet vac SYRINGE 2.5-8-5/.5 INTRAMUSC
    HIC3 W7Z
    HIC3 Description VACCINE/TOXOID PREPARATIONS,COMBINATIONS
    GCN 24619
    HICL Sequence Number 006320
    HICL Sequence Number Description DIPHTHERIA,PERTUSSIS(ACELLULAR),TETANUS VACCINE
    Brand/Generic Generic
    Proprietary Name BOOSTRIX
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed
    Product Type VACCINE
    Dosage Form SUSPENSION
    Route INTRAMUSCULAR
    Active Ingredient Strength 8; 2.5; 8; 5; 2.5
    Active Ingredient Units ug/.5mL; ug/.5mL; ug/.5mL; [iU]/.5mL; [iU]/.5mL
    Substance Name BORDETELLA PERTUSSIS FILAMENTOUS HEMAGGLUTININ ANTIGEN (FORMALDEHYDE INACTIVATED); BORDETELLA PERTUSSIS PERTACTIN ANTIGEN (FORMALDEHYDE INACTIVATED); BORDETELLA PERTUSSIS TOXOID ANTIGEN (FORMALDEHYDE, GLUTARALDEHYDE INACTIVATED); CLOSTRIDIUM TETANI TOXOID
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Actively Acquired Immunity [PE], Actively Acquired Immunity [PE], Actively Acquired Immunity [PE], Actively Acquired Immunity [PE], Actively Acquired Immunity [PE], Diphtheria Toxoid [CS], Inactivated Bordetella Pertussis Vaccine [EPC], Inactivated Bordet
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA125106
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-1377-00 (50090137700)

    NDC Package Code 50090-1377-0
    Billing NDC 50090137700
    Package 10 SYRINGE in 1 CARTON (50090-1377-0) / .5 mL in 1 SYRINGE (50090-1377-2)
    Marketing Start Date 2009-07-24
    NDC Exclude Flag N
    Pricing Information N/A