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    NDC 49281-0420-50 FLUZONE QUADRIVALENT NORTHERN HEMISPHERE 15; 15; 15; 15 ug/.5mL; ug/.5mL; ug/.5mL; ug/.5mL Details

    FLUZONE QUADRIVALENT NORTHERN HEMISPHERE 15; 15; 15; 15 ug/.5mL; ug/.5mL; ug/.5mL; ug/.5mL

    FLUZONE QUADRIVALENT NORTHERN HEMISPHERE is a INTRAMUSCULAR INJECTION, SUSPENSION in the VACCINE category. It is labeled and distributed by Sanofi Pasteur Inc.. The primary component is INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE IN.

    Product Information

    NDC 49281-0420
    Product ID 49281-420_630e666a-9196-4d8c-9b96-7ee44f4daf5f
    Associated GPIs 17100020251820 1710002025E620
    GCN Sequence Number 080986
    GCN Sequence Number Description flu vacc qs2020-21(6mos up)/PF VIAL 60MCG/.5ML INTRAMUSC
    HIC3 W7C
    HIC3 Description INFLUENZA VIRUS VACCINES
    GCN 47977
    HICL Sequence Number 046397
    HICL Sequence Number Description INFLUENZA VIRUS VACCINE QUADRIVAL 2020-2021(6 MOS AND UP)/PF
    Brand/Generic Brand
    Proprietary Name FLUZONE QUADRIVALENT NORTHERN HEMISPHERE
    Proprietary Name Suffix n/a
    Non-Proprietary Name INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED), INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED), INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE IN
    Product Type VACCINE
    Dosage Form INJECTION, SUSPENSION
    Route INTRAMUSCULAR
    Active Ingredient Strength 15; 15; 15; 15
    Active Ingredient Units ug/.5mL; ug/.5mL; ug/.5mL; ug/.5mL
    Substance Name INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/HONG KONG/2671/2019 IVR-208 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE IN
    Labeler Name Sanofi Pasteur Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA103914
    Listing Certified Through 2024-12-31

    Package

    NDC 49281-0420-50 (49281042050)

    NDC Package Code 49281-420-50
    Billing NDC 49281042050
    Package 10 SYRINGE, GLASS in 1 PACKAGE (49281-420-50) / .5 mL in 1 SYRINGE, GLASS (49281-420-88)
    Marketing Start Date 2020-07-02
    NDC Exclude Flag N
    Pricing Information N/A