Search by Drug Name or NDC

    NDC 77771-0124-30 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 RADHA PHARMACEUTICALS, INC.. The primary component is CLOPIDOGREL BISULFATE.

    Product Information

    NDC 77771-0124
    Product ID 77771-124_09ac9273-240e-b149-e063-6394a90a20cb
    Associated GPIs
    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 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 RADHA 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 77771-0124-30 (77771012430)

    NDC Package Code 77771-124-30
    Billing NDC 77771012430
    Package 30 TABLET, FILM COATED in 1 BOTTLE (77771-124-30)
    Marketing Start Date 2023-02-20
    NDC Exclude Flag N
    Pricing Information N/A