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    NDC 71767-0100-01 FUROSCIX 8 mg/mL Details

    FUROSCIX 8 mg/mL

    FUROSCIX is a SUBCUTANEOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by scPharmaceuticals Inc.. The primary component is FUROSEMIDE.

    Product Information

    NDC 71767-0100
    Product ID 71767-100_0b6532c1-7ebb-b65f-e063-6294a90a4949
    Associated GPIs
    GCN Sequence Number 083921
    GCN Sequence Number Description furosemide KIT 80 MG/10ML SUBCUT
    HIC3 R1M
    HIC3 Description LOOP DIURETICS
    GCN 52993
    HICL Sequence Number 003660
    HICL Sequence Number Description FUROSEMIDE
    Brand/Generic Brand
    Proprietary Name FUROSCIX
    Proprietary Name Suffix n/a
    Non-Proprietary Name furosemide injection 80 mg/ 10 mL
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 8
    Active Ingredient Units mg/mL
    Substance Name FUROSEMIDE
    Labeler Name scPharmaceuticals Inc.
    Pharmaceutical Class Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209988
    Listing Certified Through 2024-12-31

    Package

    NDC 71767-0100-01 (71767010001)

    NDC Package Code 71767-100-01
    Billing NDC 71767010001
    Package 1 CARTON in 1 KIT (71767-100-01) / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE
    Marketing Start Date 2022-11-14
    NDC Exclude Flag N
    Pricing Information N/A