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    NDC 68788-7616-03 Atenolol 50 mg/1 Details

    Atenolol 50 mg/1

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

    Product Information

    NDC 68788-7616
    Product ID 68788-7616_b316ff00-ae03-4d49-af08-031411ca4158
    Associated GPIs 33200020000305
    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 50
    Active Ingredient Units mg/1
    Substance Name ATENOLOL
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077443
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7616-03 (68788761603)

    NDC Package Code 68788-7616-3
    Billing NDC 68788761603
    Package 30 TABLET in 1 BOTTLE (68788-7616-3)
    Marketing Start Date 2020-02-07
    NDC Exclude Flag N
    Pricing Information N/A