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    NDC 53002-1138-00 Atenolol 100 mg/1 Details

    Atenolol 100 mg/1

    Atenolol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is ATENOLOL.

    Product Information

    NDC 53002-1138
    Product ID 53002-1138_59f5ae12-f36f-455d-a329-4d9057b42fc6
    Associated GPIs 33200020000310
    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 Atenolol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Atenolol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name ATENOLOL
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074056
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1138-00 (53002113800)

    NDC Package Code 53002-1138-0
    Billing NDC 53002113800
    Package 100 TABLET in 1 BOTTLE (53002-1138-0)
    Marketing Start Date 2018-10-01
    NDC Exclude Flag N
    Pricing Information N/A