Search by Drug Name or NDC

    NDC 53002-1653-05 Emtricitabine and Tenofovir Disoproxil Fumarate 200; 300 mg/1; mg/1 Details

    Emtricitabine and Tenofovir Disoproxil Fumarate 200; 300 mg/1; mg/1

    Emtricitabine and Tenofovir Disoproxil Fumarate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE.

    Product Information

    NDC 53002-1653
    Product ID 53002-1653_ce65bbdc-1485-4ade-93b8-a362278f4f04
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Emtricitabine and Tenofovir Disoproxil Fumarate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Emtricitabine and Tenofovir Disoproxil Fumarate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 200; 300
    Active Ingredient Units mg/1; mg/1
    Substance Name EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleosi
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090513
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1653-05 (53002165305)

    NDC Package Code 53002-1653-5
    Billing NDC 53002165305
    Package 5 TABLET, FILM COATED in 1 BOTTLE (53002-1653-5)
    Marketing Start Date 2022-01-01
    NDC Exclude Flag N
    Pricing Information N/A