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    NDC 70518-2585-00 spironolactone 50 mg/1 Details

    spironolactone 50 mg/1

    spironolactone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is SPIRONOLACTONE.

    Product Information

    NDC 70518-2585
    Product ID 70518-2585_0b63a97a-2b8d-d2b6-e063-6394a90a480a
    Associated GPIs
    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 spironolactone
    Proprietary Name Suffix n/a
    Non-Proprietary Name spironolactone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name SPIRONOLACTONE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205936
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2585-00 (70518258500)

    NDC Package Code 70518-2585-0
    Billing NDC 70518258500
    Package 30 TABLET in 1 BLISTER PACK (70518-2585-0)
    Marketing Start Date 2020-02-17
    NDC Exclude Flag N
    Pricing Information N/A