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    NDC 68788-6948-01 Furosemide 20 mg/1 Details

    Furosemide 20 mg/1

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

    Product Information

    NDC 68788-6948
    Product ID 68788-6948_a9719e77-0475-4b9f-b11e-5a060547f9d5
    Associated GPIs 37200030000305
    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 20
    Active Ingredient Units mg/1
    Substance Name FUROSEMIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077293
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-6948-01 (68788694801)

    NDC Package Code 68788-6948-1
    Billing NDC 68788694801
    Package 100 TABLET in 1 BOTTLE (68788-6948-1)
    Marketing Start Date 2017-04-17
    NDC Exclude Flag N
    Pricing Information N/A