Search by Drug Name or NDC

    NDC 68788-7297-06 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 Preferred Pharmaceuticals Inc... The primary component is SPIRONOLACTONE.

    Product Information

    NDC 68788-7297
    Product ID 68788-7297_5da00d87-d660-4548-9751-ce1f73d97bfa
    Associated GPIs 37500020000305
    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 Preferred Pharmaceuticals 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 68788-7297-06 (68788729706)

    NDC Package Code 68788-7297-6
    Billing NDC 68788729706
    Package 60 TABLET, FILM COATED in 1 BOTTLE (68788-7297-6)
    Marketing Start Date 2019-01-08
    NDC Exclude Flag N
    Pricing Information N/A