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    NDC 68788-7645-03 Clopidogrel 75 mg/1 Details

    Clopidogrel 75 mg/1

    Clopidogrel is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is CLOPIDOGREL BISULFATE.

    Product Information

    NDC 68788-7645
    Product ID 68788-7645_4f39742a-4821-46dc-ab9d-2eb1338d2c98
    Associated GPIs 85158020100320
    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
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name CLOPIDOGREL BISULFATE
    Labeler Name Preferred Pharmaceuticals Inc.
    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 ANDA202928
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7645-03 (68788764503)

    NDC Package Code 68788-7645-3
    Billing NDC 68788764503
    Package 30 TABLET in 1 BOTTLE (68788-7645-3)
    Marketing Start Date 2020-11-03
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e0e66d6e-76bc-4a8e-81c1-5b8b190fe97a Details

    Revised: 4/2022