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    NDC 61958-1003-02 Ranexa 500 mg/1 Details

    Ranexa 500 mg/1

    Ranexa is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Gilead Sciences, Inc.. The primary component is RANOLAZINE.

    Product Information

    NDC 61958-1003
    Product ID 61958-1003_ba1f4469-5e3c-447a-9d28-8e57a2c32a17
    Associated GPIs 32200040007420
    GCN Sequence Number 060333
    GCN Sequence Number Description ranolazine TAB ER 12H 500 MG ORAL
    HIC3 A2C
    HIC3 Description ANTIANGINAL, ANTI-ISCHEMIC AGENTS,NON-HEMODYNAMIC
    GCN 26459
    HICL Sequence Number 033446
    HICL Sequence Number Description RANOLAZINE
    Brand/Generic Brand
    Proprietary Name Ranexa
    Proprietary Name Suffix n/a
    Non-Proprietary Name RANOLAZINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name RANOLAZINE
    Labeler Name Gilead Sciences, Inc.
    Pharmaceutical Class Anti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021526
    Listing Certified Through 2022-12-31

    Package

    NDC 61958-1003-02 (61958100302)

    NDC Package Code 61958-1003-2
    Billing NDC 61958100302
    Package 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (61958-1003-2)
    Marketing Start Date 2006-01-27
    NDC Exclude Flag N
    Pricing Information N/A