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    NDC 51655-0713-25 Carvedilol 3.125 mg/1 Details

    Carvedilol 3.125 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 51655-0713
    Product ID 51655-713_db5d9e6c-6565-b0f7-e053-2995a90a77f2
    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 3.125
    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 ANDA078384
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0713-25 (51655071325)

    NDC Package Code 51655-713-25
    Billing NDC 51655071325
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-25)
    Marketing Start Date 2022-04-15
    NDC Exclude Flag N
    Pricing Information N/A