Search by Drug Name or NDC

    NDC 49281-0422-10 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/DARWIN/9/2021 SAN-010 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MICHIGAN/01/2021 ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUEN.

    Product Information

    NDC 49281-0422
    Product ID 49281-422_630e666a-9196-4d8c-9b96-7ee44f4daf5f
    Associated GPIs
    GCN Sequence Number 083293
    GCN Sequence Number Description flu vacc qs2022-23(6mos up)/PF VIAL 60MCG/.5ML INTRAMUSC
    HIC3 W7C
    HIC3 Description INFLUENZA VIRUS VACCINES
    GCN 52204
    HICL Sequence Number 047932
    HICL Sequence Number Description INFLUENZA VIRUS VACCINE QUADRIVAL 2022-2023(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/Victoria/2570/2019 IVR-215 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED), INFLUENZA A VIRUS A/DARWIN/9/2021 SAN-010 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED), INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED), and INF
    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/DARWIN/9/2021 SAN-010 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/VICTORIA/2570/2019 IVR-215 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MICHIGAN/01/2021 ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUEN
    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 49281-0422-10 (49281042210)

    NDC Package Code 49281-422-10
    Billing NDC 49281042210
    Package 10 VIAL, SINGLE-DOSE in 1 PACKAGE (49281-422-10) / .5 mL in 1 VIAL, SINGLE-DOSE (49281-422-58)
    Marketing Start Date 2022-07-01
    NDC Exclude Flag N
    Pricing Information N/A