Search by Drug Name or NDC

    NDC 72865-0231-60 Maraviroc 150 mg/1 Details

    Maraviroc 150 mg/1

    Maraviroc is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by XLCare Pharmaceuticals Inc.. The primary component is MARAVIROC.

    Product Information

    NDC 72865-0231
    Product ID 72865-231_00498e1e-2c96-4932-e063-6294a90abfc4
    Associated GPIs
    GCN Sequence Number 062974
    GCN Sequence Number Description maraviroc TABLET 150 MG ORAL
    HIC3 W5T
    HIC3 Description ANTIVIRALS, HIV-SPECIFIC, CCR5 CO-RECEPTOR ANTAG.
    GCN 98734
    HICL Sequence Number 034927
    HICL Sequence Number Description MARAVIROC
    Brand/Generic Generic
    Proprietary Name Maraviroc
    Proprietary Name Suffix n/a
    Non-Proprietary Name Maraviroc
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 150
    Active Ingredient Units mg/1
    Substance Name MARAVIROC
    Labeler Name XLCare Pharmaceuticals Inc.
    Pharmaceutical Class CCR5 Co-receptor Antagonist [EPC], Chemokine Co-receptor 5 Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203347
    Listing Certified Through 2024-12-31

    Package

    NDC 72865-0231-60 (72865023160)

    NDC Package Code 72865-231-60
    Billing NDC 72865023160
    Package 60 TABLET, FILM COATED in 1 BOTTLE (72865-231-60)
    Marketing Start Date 2023-06-01
    NDC Exclude Flag N
    Pricing Information N/A