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    NDC 49702-0217-18 TRIZIVIR 300; 150; 300 mg/1; mg/1; mg/1 Details

    TRIZIVIR 300; 150; 300 mg/1; mg/1; mg/1

    TRIZIVIR is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ViiV Healthcare Company. The primary component is ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE.

    Product Information

    NDC 49702-0217
    Product ID 49702-217_82d4603e-fbba-4bf5-8946-b279d775dd46
    Associated GPIs 12109903200320
    GCN Sequence Number 047121
    GCN Sequence Number Description abacavir/lamivudine/zidovudine TABLET 150-300 MG ORAL
    HIC3 W5L
    HIC3 Description ANTIVIRALS, HIV-SPEC., NUCLEOSIDE ANALOG, RTI COMB
    GCN 87691
    HICL Sequence Number 021800
    HICL Sequence Number Description ABACAVIR SULFATE/LAMIVUDINE/ZIDOVUDINE
    Brand/Generic Brand
    Proprietary Name TRIZIVIR
    Proprietary Name Suffix n/a
    Non-Proprietary Name abacavir sulfate, lamivudine, and zidovudine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 300; 150; 300
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ABACAVIR SULFATE; LAMIVUDINE; ZIDOVUDINE
    Labeler Name ViiV Healthcare Company
    Pharmaceutical Class Cytochrome P450 1A1 Inhibitors [MoA], Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse T
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021205
    Listing Certified Through 2024-12-31

    Package

    NDC 49702-0217-18 (49702021718)

    NDC Package Code 49702-217-18
    Billing NDC 49702021718
    Package 60 TABLET, FILM COATED in 1 BOTTLE (49702-217-18)
    Marketing Start Date 2010-11-02
    NDC Exclude Flag N
    Pricing Information N/A