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    NDC 68788-7700-06 Clopidogrel bisulfate 75 mg/1 Details

    Clopidogrel bisulfate 75 mg/1

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

    Product Information

    NDC 68788-7700
    Product ID 68788-7700_c3470464-9722-41b3-855c-33113a5d7521
    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 bisulfate
    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 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 ANDA204165
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7700-06 (68788770006)

    NDC Package Code 68788-7700-6
    Billing NDC 68788770006
    Package 60 TABLET, FILM COATED in 1 BOTTLE (68788-7700-6)
    Marketing Start Date 2020-05-01
    NDC Exclude Flag N
    Pricing Information N/A