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    NDC 76420-0062-01 Spironolactone 25 mg/1 Details

    Spironolactone 25 mg/1

    Spironolactone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is SPIRONOLACTONE.

    Product Information

    NDC 76420-0062
    Product ID 76420-062_06c94882-1323-c834-e063-6394a90a2d75
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name SPIRONOLACTONE
    Labeler Name Asclemed USA, Inc.
    Pharmaceutical Class Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203512
    Listing Certified Through 2024-12-31

    Package

    NDC 76420-0062-01 (76420006201)

    NDC Package Code 76420-062-01
    Billing NDC 76420006201
    Package 100 TABLET, FILM COATED in 1 BOTTLE (76420-062-01)
    Marketing Start Date 2023-10-03
    NDC Exclude Flag N
    Pricing Information N/A