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    NDC 68788-8177-03 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 Preferred Pharmaceuticals Inc.. The primary component is CARVEDILOL.

    Product Information

    NDC 68788-8177
    Product ID 68788-8177_a6567980-c9d2-4fc9-9305-98edc520e018
    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 Preferred 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 ANDA078165
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8177-03 (68788817703)

    NDC Package Code 68788-8177-3
    Billing NDC 68788817703
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-8177-3)
    Marketing Start Date 2022-04-28
    NDC Exclude Flag N
    Pricing Information N/A