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    NDC 00069-8141-20 Xalkori 200 mg/1 Details

    Xalkori 200 mg/1

    Xalkori is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is CRIZOTINIB.

    Product Information

    NDC 00069-8141
    Product ID 0069-8141_e4384d2f-d204-468c-a2d4-23666e3a493f
    Associated GPIs 21530517000120
    GCN Sequence Number 067824
    GCN Sequence Number Description crizotinib CAPSULE 200 MG ORAL
    HIC3 V1Q
    HIC3 Description ANTINEOPLASTIC SYSTEMIC ENZYME INHIBITORS
    GCN 30458
    HICL Sequence Number 037916
    HICL Sequence Number Description CRIZOTINIB
    Brand/Generic Brand
    Proprietary Name Xalkori
    Proprietary Name Suffix n/a
    Non-Proprietary Name CRIZOTINIB
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CRIZOTINIB
    Labeler Name Pfizer Laboratories Div Pfizer Inc
    Pharmaceutical Class Cytochrome P450 2B6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], Organic Cation Transporter 1 Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA], Receptor Tyrosine Kinase Inhi
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA202570
    Listing Certified Through 2024-12-31

    Package

    NDC 00069-8141-20 (00069814120)

    NDC Package Code 0069-8141-20
    Billing NDC 00069814120
    Package 60 CAPSULE in 1 BOTTLE (0069-8141-20)
    Marketing Start Date 2011-08-26
    NDC Exclude Flag N
    Pricing Information N/A