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    NDC 61919-0007-30 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 DIRECT RX. The primary component is CLOPIDOGREL BISULFATE.

    Product Information

    NDC 61919-0007
    Product ID 61919-007_f80e7872-5b20-fb4b-e053-6294a90ae2b3
    Associated GPIs 85158020100320
    GCN Sequence Number 038164
    GCN Sequence Number Description clopidogrel bisulfate TABLET 75 MG ORAL
    HIC3 M9P
    HIC3 Description PLATELET AGGREGATION INHIBITORS
    GCN 96010
    HICL Sequence Number 017539
    HICL Sequence Number Description CLOPIDOGREL BISULFATE
    Brand/Generic Generic
    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 DIRECT RX
    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 61919-0007-30 (61919000730)

    NDC Package Code 61919-007-30
    Billing NDC 61919000730
    Package 30 TABLET, FILM COATED in 1 BOTTLE (61919-007-30)
    Marketing Start Date 2020-06-18
    NDC Exclude Flag N
    Pricing Information N/A