Search by Drug Name or NDC

    NDC 71335-0080-03 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 71335-0080
    Product ID 71335-0080_27661b2a-5453-4078-8329-10ea715abcef
    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 Bisulfate
    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 ANDA090540
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0080-03 (71335008003)

    NDC Package Code 71335-0080-3
    Billing NDC 71335008003
    Package 60 TABLET, FILM COATED in 1 BOTTLE (71335-0080-3)
    Marketing Start Date 2021-12-27
    NDC Exclude Flag N
    Pricing Information N/A