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    NDC 70710-1049-03 Abacavir and lamivudine 600; 300 mg/1; mg/1 Details

    Abacavir and lamivudine 600; 300 mg/1; mg/1

    Abacavir and lamivudine is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is ABACAVIR SULFATE; LAMIVUDINE.

    Product Information

    NDC 70710-1049
    Product ID 70710-1049_35bd1a78-3b48-4df3-ac63-6f5f14816922
    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 Abacavir and lamivudine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Abacavir and lamivudine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 600; 300
    Active Ingredient Units mg/1; mg/1
    Substance Name ABACAVIR SULFATE; LAMIVUDINE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    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 ANDA
    Application Number ANDA208990
    Listing Certified Through 2024-12-31

    Package

    NDC 70710-1049-03 (70710104903)

    NDC Package Code 70710-1049-3
    Billing NDC 70710104903
    Package 30 TABLET, FILM COATED in 1 BOTTLE (70710-1049-3)
    Marketing Start Date 2019-03-14
    NDC Exclude Flag N
    Pricing Information N/A