Search by Drug Name or NDC

    NDC 43063-0716-30 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 PD-Rx Pharmaceuticals, Inc.. The primary component is FUROSEMIDE.

    Product Information

    NDC 43063-0716
    Product ID 43063-716_f99eece6-1b80-9866-e053-6394a90a23c6
    Associated GPIs 37200030000310
    GCN Sequence Number 008209
    GCN Sequence Number Description furosemide TABLET 40 MG ORAL
    HIC3 R1M
    HIC3 Description LOOP DIURETICS
    GCN 34962
    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 40
    Active Ingredient Units mg/1
    Substance Name FUROSEMIDE
    Labeler Name PD-Rx 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 43063-0716-30 (43063071630)

    NDC Package Code 43063-716-30
    Billing NDC 43063071630
    Package 30 TABLET in 1 BOTTLE, PLASTIC (43063-716-30)
    Marketing Start Date 2016-10-12
    NDC Exclude Flag N
    Pricing Information N/A