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    NDC 68788-7206-09 Metoprolol Succinate 25 mg/1 Details

    Metoprolol Succinate 25 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 68788-7206
    Product ID 68788-7206_0b5e7702-3244-41de-b108-f8dba952ffb4
    Associated GPIs 33200030057510
    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 25
    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 ANDA204106
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7206-09 (68788720609)

    NDC Package Code 68788-7206-9
    Billing NDC 68788720609
    Package 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7206-9)
    Marketing Start Date 2018-08-06
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 866439a7-b1b7-4c23-bc99-cbf78440f8db Details

    Revised: 9/2022