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    NDC 57664-0162-58 Metoprolol tartrate 100 mg/1 Details

    Metoprolol tartrate 100 mg/1

    Metoprolol tartrate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is METOPROLOL TARTRATE.

    Product Information

    NDC 57664-0162
    Product ID 57664-162_0e91f855-67c8-037b-e063-6294a90a0a54
    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
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name METOPROLOL TARTRATE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074644
    Listing Certified Through 2025-12-31

    Package

    NDC 57664-0162-58 (57664016258)

    NDC Package Code 57664-162-58
    Billing NDC 57664016258
    Package 1000 TABLET in 1 BOTTLE (57664-162-58)
    Marketing Start Date 2015-06-29
    NDC Exclude Flag N
    Pricing Information N/A
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