Search by Drug Name or NDC

    NDC 16714-0638-01 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 NorthStar RxLLC. The primary component is SPIRONOLACTONE.

    Product Information

    NDC 16714-0638
    Product ID 16714-638_ee4b013a-434e-77ae-e053-2a95a90a1c6d
    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 NorthStar RxLLC
    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 16714-0638-01 (16714063801)

    NDC Package Code 16714-638-01
    Billing NDC 16714063801
    Package 100 TABLET, FILM COATED in 1 BOTTLE (16714-638-01)
    Marketing Start Date 2022-11-18
    NDC Exclude Flag N
    Pricing Information N/A
    << 16714-0637-03 16714-0638-02 >>

    Contents