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    NDC 63739-0178-30 Clopidogrel bisulfate 300 mg/1 Details

    Clopidogrel bisulfate 300 mg/1

    Clopidogrel bisulfate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by McKesson Corporation dba SKY Packaging. The primary component is CLOPIDOGREL BISULFATE.

    Product Information

    NDC 63739-0178
    Product ID 63739-178_46c30fc8-7591-a7fb-a93e-34e807b32c4b
    Associated GPIs
    GCN Sequence Number 063544
    GCN Sequence Number Description clopidogrel bisulfate TABLET 300 MG ORAL
    HIC3 M9P
    HIC3 Description PLATELET AGGREGATION INHIBITORS
    GCN 99266
    HICL Sequence Number 017539
    HICL Sequence Number Description CLOPIDOGREL BISULFATE
    Brand/Generic Generic
    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 300
    Active Ingredient Units mg/1
    Substance Name CLOPIDOGREL BISULFATE
    Labeler Name McKesson Corporation dba SKY Packaging
    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 ANDA091023
    Listing Certified Through 2024-12-31

    Package

    NDC 63739-0178-30 (63739017830)

    NDC Package Code 63739-178-30
    Billing NDC 63739017830
    Package 5 BLISTER PACK in 1 CARTON (63739-178-30) / 6 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2022-08-18
    NDC Exclude Flag N
    Pricing Information N/A