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    NDC 63629-4728-01 Clopidogrel 75 mg/1 Details

    Clopidogrel 75 mg/1

    Clopidogrel is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CLOPIDOGREL BISULFATE.

    Product Information

    NDC 63629-4728
    Product ID 63629-4728_4a22874a-ae21-4da8-b1c5-6732e9b00825
    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 Clopidogrel
    Proprietary Name Suffix n/a
    Non-Proprietary Name Clopidogrel
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name CLOPIDOGREL BISULFATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076999
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-4728-01 (63629472801)

    NDC Package Code 63629-4728-1
    Billing NDC 63629472801
    Package 90 TABLET, FILM COATED in 1 BOTTLE (63629-4728-1)
    Marketing Start Date 2012-05-29
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 4a22874a-ae21-4da8-b1c5-6732e9b00825 Details

    Revised: 2/2022