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    NDC 68788-7997-09 metoprolol succinate 50 mg/1 Details

    metoprolol succinate 50 mg/1

    metoprolol succinate is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is METOPROLOL SUCCINATE.

    Product Information

    NDC 68788-7997
    Product ID 68788-7997_3b93ee74-6b0a-454f-92ea-364037bfdf3b
    Associated GPIs 33200030057520
    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 metoprolol succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name metoprolol succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name METOPROLOL SUCCINATE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203894
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7997-09 (68788799709)

    NDC Package Code 68788-7997-9
    Billing NDC 68788799709
    Package 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7997-9)
    Marketing Start Date 2021-08-10
    NDC Exclude Flag N
    Pricing Information N/A