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    NDC 68462-0163-60 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 Glenmark Pharmaceuticals Inc., USA. The primary component is CARVEDILOL.

    Product Information

    NDC 68462-0163
    Product ID 68462-163_2155a4b3-b3d1-4dba-81d9-b8b7f7fe2cce
    Associated GPIs 33300007000310
    GCN Sequence Number 028109
    GCN Sequence Number Description carvedilol TABLET 6.25 MG ORAL
    HIC3 J7A
    HIC3 Description ALPHA/BETA-ADRENERGIC BLOCKING AGENTS
    GCN 01554
    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 6.25
    Active Ingredient Units mg/1
    Substance Name CARVEDILOL
    Labeler Name Glenmark Pharmaceuticals Inc., USA
    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 ANDA078251
    Listing Certified Through 2024-12-31

    Package

    NDC 68462-0163-60 (68462016360)

    NDC Package Code 68462-163-60
    Billing NDC 68462016360
    Package 60 TABLET, FILM COATED in 1 BOTTLE (68462-163-60)
    Marketing Start Date 2007-09-05
    NDC Exclude Flag N
    Pricing Information N/A