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    NDC 68788-7910-01 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 Preferred Pharmaceuticals Inc.,. The primary component is CARVEDILOL.

    Product Information

    NDC 68788-7910
    Product ID 68788-7910_812a2f68-9c5a-4448-946a-77db8215000a
    Associated GPIs 33300007000330
    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 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 ANDA078251
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7910-01 (68788791001)

    NDC Package Code 68788-7910-1
    Billing NDC 68788791001
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68788-7910-1)
    Marketing Start Date 2022-04-12
    NDC Exclude Flag N
    Pricing Information N/A