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    NDC 50090-1856-01 Carvedilol 3.125 mg/1 Details

    Carvedilol 3.125 mg/1

    Carvedilol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is CARVEDILOL.

    Product Information

    NDC 50090-1856
    Product ID 50090-1856_894e1d7f-9c2b-4a8d-b32e-2745c7291e20
    Associated GPIs 33300007000305
    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 Carvedilol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Carvedilol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 3.125
    Active Ingredient Units mg/1
    Substance Name CARVEDILOL
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078332
    Listing Certified Through 2024-12-31

    Package

    NDC 50090-1856-01 (50090185601)

    NDC Package Code 50090-1856-1
    Billing NDC 50090185601
    Package 180 TABLET, FILM COATED in 1 BOTTLE (50090-1856-1)
    Marketing Start Date 2015-06-02
    NDC Exclude Flag N
    Pricing Information N/A