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    NDC 71335-0561-04 Carvedilol 6.25 mg/1 Details

    Carvedilol 6.25 mg/1

    Carvedilol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CARVEDILOL.

    Product Information

    NDC 71335-0561
    Product ID 71335-0561_787fea0c-edad-4b3d-96d9-00b9a298a211
    Associated GPIs 33300007000310
    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 6.25
    Active Ingredient Units mg/1
    Substance Name CARVEDILOL
    Labeler Name Bryant Ranch Prepack
    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 2023-12-31

    Package

    NDC 71335-0561-04 (71335056104)

    NDC Package Code 71335-0561-4
    Billing NDC 71335056104
    Package 180 TABLET, FILM COATED in 1 BOTTLE (71335-0561-4)
    Marketing Start Date 2018-05-24
    NDC Exclude Flag N
    Pricing Information N/A