Search by Drug Name or NDC

    NDC 68788-7265-03 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 68788-7265
    Product ID 68788-7265_afc689af-7530-4305-a162-ab9493d5814e
    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 ANDA076796
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7265-03 (68788726503)

    NDC Package Code 68788-7265-3
    Billing NDC 68788726503
    Package 30 TABLET in 1 BOTTLE, PLASTIC (68788-7265-3)
    Marketing Start Date 2018-09-24
    NDC Exclude Flag N
    Pricing Information N/A