Search by Drug Name or NDC

    NDC 50268-0184-12 Clopidogrel 300 mg/1 Details

    Clopidogrel 300 mg/1

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

    Product Information

    NDC 50268-0184
    Product ID 50268-184_0e85fc4a-96b8-b715-e063-6294a90a22e6
    Associated GPIs 85158020100340
    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
    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 AvPAK
    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 2025-12-31

    Package

    NDC 50268-0184-12 (50268018412)

    NDC Package Code 50268-184-12
    Billing NDC 50268018412
    Package 20 BLISTER PACK in 1 BOX (50268-184-12) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-184-11)
    Marketing Start Date 2019-10-11
    NDC Exclude Flag N
    Pricing Information N/A