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    NDC 63187-0609-90 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 Proficient Rx LP. The primary component is METOPROLOL TARTRATE.

    Product Information

    NDC 63187-0609
    Product ID 63187-609_a5cdde79-e69c-49ab-bdf6-31224a110e38
    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 Proficient Rx LP
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077739
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0609-90 (63187060990)

    NDC Package Code 63187-609-90
    Billing NDC 63187060990
    Package 90 TABLET, FILM COATED in 1 BOTTLE (63187-609-90)
    Marketing Start Date 2018-12-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d4c8f068-7410-4543-9a66-7f4c19ff63a5 Details

    Revised: 4/2022