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    NDC 42385-0962-18 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 Laurus Labs Limited. The primary component is ABACAVIR SULFATE; LAMIVUDINE.

    Product Information

    NDC 42385-0962
    Product ID 42385-962_0c1a2d90-e5e1-48ff-8e81-7d2bec0e50d0
    Associated GPIs
    GCN Sequence Number 057896
    GCN Sequence Number Description abacavir sulfate/lamivudine TABLET 600-300 MG ORAL
    HIC3 W5L
    HIC3 Description ANTIVIRALS, HIV-SPEC., NUCLEOSIDE ANALOG, RTI COMB
    GCN 23167
    HICL Sequence Number 026524
    HICL Sequence Number Description ABACAVIR SULFATE/LAMIVUDINE
    Brand/Generic Generic
    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 Laurus Labs Limited
    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 ANDA216332
    Listing Certified Through 2024-12-31

    Package

    NDC 42385-0962-18 (42385096218)

    NDC Package Code 42385-962-18
    Billing NDC 42385096218
    Package 180 TABLET, FILM COATED in 1 BOTTLE (42385-962-18)
    Marketing Start Date 2022-07-25
    NDC Exclude Flag N
    Pricing Information N/A