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    NDC 30698-0630-01 Bumex 0.5 mg/1 Details

    Bumex 0.5 mg/1

    Bumex is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Validus Pharmaceuticals LLC. The primary component is BUMETANIDE.

    Product Information

    NDC 30698-0630
    Product ID 30698-630_ef39d792-2e46-40a9-b0ac-c2fc34a93ba0
    Associated GPIs 37200010000305
    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 Bumex
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bumetanide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name BUMETANIDE
    Labeler Name Validus Pharmaceuticals LLC
    Pharmaceutical Class Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA018225
    Listing Certified Through 2024-12-31

    Package

    NDC 30698-0630-01 (30698063001)

    NDC Package Code 30698-630-01
    Billing NDC 30698063001
    Package 100 TABLET in 1 BOTTLE (30698-630-01)
    Marketing Start Date 1983-02-28
    NDC Exclude Flag N
    Pricing Information N/A