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    NDC 67877-0593-05 Metoprolol Succinate 200 mg/1 Details

    Metoprolol Succinate 200 mg/1

    Metoprolol Succinate is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is METOPROLOL SUCCINATE.

    Product Information

    NDC 67877-0593
    Product ID 67877-593_702d0174-8053-45b2-81bf-ef33162a7184
    Associated GPIs 33200030057540
    GCN Sequence Number 016601
    GCN Sequence Number Description metoprolol succinate TAB ER 24H 200 MG ORAL
    HIC3 J7C
    HIC3 Description BETA-ADRENERGIC BLOCKING AGENTS
    GCN 20743
    HICL Sequence Number 006323
    HICL Sequence Number Description METOPROLOL SUCCINATE
    Brand/Generic Generic
    Proprietary Name Metoprolol Succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metoprolol Succinate ER Tablets
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name METOPROLOL SUCCINATE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211143
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0593-05 (67877059305)

    NDC Package Code 67877-593-05
    Billing NDC 67877059305
    Package 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-593-05)
    Marketing Start Date 2020-11-27
    NDC Exclude Flag N
    Pricing Information N/A