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    NDC 68001-0314-08 Lovastatin 10 mg/1 Details

    Lovastatin 10 mg/1

    Lovastatin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by BluePoint Laboratories. The primary component is LOVASTATIN.

    Product Information

    NDC 68001-0314
    Product ID 68001-314_00ff832a-bce0-29bf-e063-6294a90a3d71
    Associated GPIs 39400050000305
    GCN Sequence Number 016310
    GCN Sequence Number Description lovastatin TABLET 10 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 47042
    HICL Sequence Number 002793
    HICL Sequence Number Description LOVASTATIN
    Brand/Generic Generic
    Proprietary Name Lovastatin
    Proprietary Name Suffix n/a
    Non-Proprietary Name lovastatin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name LOVASTATIN
    Labeler Name BluePoint Laboratories
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078296
    Listing Certified Through 2024-12-31

    Package

    NDC 68001-0314-08 (68001031408)

    NDC Package Code 68001-314-08
    Billing NDC 68001031408
    Package 1000 TABLET in 1 BOTTLE (68001-314-08)
    Marketing Start Date 2017-02-07
    NDC Exclude Flag N
    Pricing Information N/A