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    NDC 63629-5341-06 SPIRONOLACTONE 50 mg/1 Details

    SPIRONOLACTONE 50 mg/1

    SPIRONOLACTONE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is SPIRONOLACTONE.

    Product Information

    NDC 63629-5341
    Product ID 63629-5341_ed6e23ec-657b-4b09-a3a7-84174eb223e9
    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 50
    Active Ingredient Units mg/1
    Substance Name SPIRONOLACTONE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA089424
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-5341-06 (63629534106)

    NDC Package Code 63629-5341-6
    Billing NDC 63629534106
    Package 10 TABLET, FILM COATED in 1 BOTTLE (63629-5341-6)
    Marketing Start Date 2023-03-09
    NDC Exclude Flag N
    Pricing Information N/A