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    NDC 43063-0126-60 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 PD-Rx Pharmaceuticals, Inc.. The primary component is CARVEDILOL.

    Product Information

    NDC 43063-0126
    Product ID 43063-126_f56420b6-16f2-3ff6-e053-2a95a90a00b5
    Associated GPIs 33300007000305
    GCN Sequence Number 028108
    GCN Sequence Number Description carvedilol TABLET 3.125 MG ORAL
    HIC3 J7A
    HIC3 Description ALPHA/BETA-ADRENERGIC BLOCKING AGENTS
    GCN 01553
    HICL Sequence Number 013795
    HICL Sequence Number Description CARVEDILOL
    Brand/Generic Generic
    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 PD-Rx Pharmaceuticals, Inc.
    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 43063-0126-60 (43063012660)

    NDC Package Code 43063-126-60
    Billing NDC 43063012660
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-126-60)
    Marketing Start Date 2013-10-30
    NDC Exclude Flag N
    Pricing Information N/A