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    NDC 70121-1164-05 Furosemide 40 mg/4mL Details

    Furosemide 40 mg/4mL

    Furosemide is a INTRAMUSCULAR; INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is FUROSEMIDE.

    Product Information

    NDC 70121-1164
    Product ID 70121-1164_ea35ac1b-9376-43dd-a285-64954995e9b6
    Associated GPIs 37200030002005
    GCN Sequence Number 008205
    GCN Sequence Number Description furosemide VIAL 10 MG/ML INJECTION
    HIC3 R1M
    HIC3 Description LOOP DIURETICS
    GCN 34940
    HICL Sequence Number 003660
    HICL Sequence Number Description FUROSEMIDE
    Brand/Generic Generic
    Proprietary Name Furosemide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Furosemide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 40
    Active Ingredient Units mg/4mL
    Substance Name FUROSEMIDE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207552
    Listing Certified Through 2024-12-31

    Package

    NDC 70121-1164-05 (70121116405)

    NDC Package Code 70121-1164-5
    Billing NDC 70121116405
    Package 25 VIAL, GLASS in 1 CARTON (70121-1164-5) / 4 mL in 1 VIAL, GLASS (70121-1164-1)
    Marketing Start Date 2016-07-25
    NDC Exclude Flag N
    Pricing Information N/A