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    NDC 51655-0397-83 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 Northwind Pharmaceuticals. The primary component is CARVEDILOL.

    Product Information

    NDC 51655-0397
    Product ID 51655-397_d9c9fd0e-7801-8068-e053-2995a90a5bb9
    Associated GPIs
    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 Northwind Pharmaceuticals
    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 51655-0397-83 (51655039783)

    NDC Package Code 51655-397-83
    Billing NDC 51655039783
    Package 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-397-83)
    Marketing Start Date 2023-03-10
    NDC Exclude Flag N
    Pricing Information N/A