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    NDC 42291-0470-01 Furosemide 80 mg/1 Details

    Furosemide 80 mg/1

    Furosemide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is FUROSEMIDE.

    Product Information

    NDC 42291-0470
    Product ID 42291-470_0e8ff8ef-59bc-df59-e063-6394a90a9e20
    Associated GPIs 37200030000315
    GCN Sequence Number 008210
    GCN Sequence Number Description furosemide TABLET 80 MG ORAL
    HIC3 R1M
    HIC3 Description LOOP DIURETICS
    GCN 34963
    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 TABLET
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/1
    Substance Name FUROSEMIDE
    Labeler Name AvKARE
    Pharmaceutical Class Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076796
    Listing Certified Through 2025-12-31

    Package

    NDC 42291-0470-01 (42291047001)

    NDC Package Code 42291-470-01
    Billing NDC 42291047001
    Package 100 TABLET in 1 BOTTLE (42291-470-01)
    Marketing Start Date 2022-01-04
    NDC Exclude Flag N
    Pricing Information N/A