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    NDC 68382-0095-17 Carvedilol 25 mg/1 Details

    Carvedilol 25 mg/1

    Carvedilol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is CARVEDILOL.

    Product Information

    NDC 68382-0095
    Product ID 68382-095_2e368267-8da4-4606-9348-0246a064016c
    Associated GPIs 33300007000330
    GCN Sequence Number 019293
    GCN Sequence Number Description carvedilol TABLET 25 MG ORAL
    HIC3 J7A
    HIC3 Description ALPHA/BETA-ADRENERGIC BLOCKING AGENTS
    GCN 01551
    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 25
    Active Ingredient Units mg/1
    Substance Name CARVEDILOL
    Labeler Name Zydus Pharmaceuticals USA 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 ANDA077614
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0095-17 (68382009517)

    NDC Package Code 68382-095-17
    Billing NDC 68382009517
    Package 28 TABLET, FILM COATED in 1 BOTTLE (68382-095-17)
    Marketing Start Date 2007-09-05
    NDC Exclude Flag N
    Pricing Information N/A