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    NDC 55154-5512-00 Metoprolol Tartrate 50 mg/1 Details

    Metoprolol Tartrate 50 mg/1

    Metoprolol Tartrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is METOPROLOL TARTRATE.

    Product Information

    NDC 55154-5512
    Product ID 55154-5512_0bc82d06-7e35-4c5c-9c81-5f0b61ac6db3
    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 Metoprolol Tartrate
    Proprietary Name Suffix n/a
    Non-Proprietary Name metoprolol tartrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name METOPROLOL TARTRATE
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076704
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-5512-00 (55154551200)

    NDC Package Code 55154-5512-0
    Billing NDC 55154551200
    Package 10 BLISTER PACK in 1 BAG (55154-5512-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 1994-05-03
    NDC Exclude Flag N
    Pricing Information N/A