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    NDC 50458-0579-99 Xarelto 20 mg/1 Details

    Xarelto 20 mg/1

    Xarelto is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Janssen Pharmaceuticals, Inc.. The primary component is RIVAROXABAN.

    Product Information

    NDC 50458-0579
    Product ID 50458-579_0aaf0811-077b-1625-e063-6394a90a9177
    Associated GPIs 83370060000340
    GCN Sequence Number 068119
    GCN Sequence Number Description rivaroxaban TABLET 20 MG ORAL
    HIC3 M9V
    HIC3 Description DIRECT FACTOR XA INHIBITORS
    GCN 30819
    HICL Sequence Number 035915
    HICL Sequence Number Description RIVAROXABAN
    Brand/Generic Brand
    Proprietary Name Xarelto
    Proprietary Name Suffix n/a
    Non-Proprietary Name rivaroxaban
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name RIVAROXABAN
    Labeler Name Janssen Pharmaceuticals, Inc.
    Pharmaceutical Class Factor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA022406
    Listing Certified Through 2024-12-31

    Package

    NDC 50458-0579-99 (50458057999)

    NDC Package Code 50458-579-99
    Billing NDC 50458057999
    Package 5 TABLET, FILM COATED in 1 BOTTLE (50458-579-99)
    Marketing Start Date 2011-11-05
    NDC Exclude Flag N
    Pricing Information N/A