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    NDC 71205-0146-30 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 Proficient Rx LP. The primary component is SPIRONOLACTONE.

    Product Information

    NDC 71205-0146
    Product ID 71205-146_5857334b-cd0a-47c8-ba29-b8ba367162fa
    Associated GPIs 37500020000305
    GCN Sequence Number 006817
    GCN Sequence Number Description spironolactone TABLET 25 MG ORAL
    HIC3 R1H
    HIC3 Description POTASSIUM SPARING DIURETICS
    GCN 27691
    HICL Sequence Number 002901
    HICL Sequence Number Description SPIRONOLACTONE
    Brand/Generic Generic
    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 Proficient Rx LP
    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 71205-0146-30 (71205014630)

    NDC Package Code 71205-146-30
    Billing NDC 71205014630
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-146-30)
    Marketing Start Date 2018-11-01
    NDC Exclude Flag N
    Pricing Information N/A