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    NDC 68788-7539-03 Carvedilol 12.5 mg/1 Details

    Carvedilol 12.5 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 68788-7539
    Product ID 68788-7539_eaeb433f-752a-41f7-8ecb-9b367d5c266c
    Associated GPIs 33300007000320
    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 12.5
    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 ANDA077614
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7539-03 (68788753903)

    NDC Package Code 68788-7539-3
    Billing NDC 68788753903
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-7539-3)
    Marketing Start Date 2019-12-27
    NDC Exclude Flag N
    Pricing Information N/A