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    NDC 71335-0842-01 Furosemide 40 mg/1 Details

    Furosemide 40 mg/1

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

    Product Information

    NDC 71335-0842
    Product ID 71335-0842_fc767667-70ab-0fce-e053-6394a90a9831
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 40
    Active Ingredient Units mg/1
    Substance Name FUROSEMIDE
    Labeler Name Bryant Ranch Prepack
    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 2024-12-31

    Package

    NDC 71335-0842-01 (71335084201)

    NDC Package Code 71335-0842-1
    Billing NDC 71335084201
    Package 40 TABLET in 1 BOTTLE (71335-0842-1)
    Marketing Start Date 2018-05-31
    NDC Exclude Flag N
    Pricing Information N/A