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    NDC 70934-0111-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is FUROSEMIDE.

    Product Information

    NDC 70934-0111
    Product ID 70934-111_d101bc44-8d7d-0481-e053-2995a90a294b
    Associated GPIs 37200030000305
    GCN Sequence Number 008208
    GCN Sequence Number Description furosemide TABLET 20 MG ORAL
    HIC3 R1M
    HIC3 Description LOOP DIURETICS
    GCN 34961
    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 20
    Active Ingredient Units mg/1
    Substance Name FUROSEMIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0111-30 (70934011130)

    NDC Package Code 70934-111-30
    Billing NDC 70934011130
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-111-30)
    Marketing Start Date 2018-05-16
    NDC Exclude Flag N
    Pricing Information N/A